Transcript reference sequence [ID]   51958-7

LOINC Code


LOINC code51958-7
nameTranscript reference sequence [ID]
descriptionThis field carries the ID for the transcribed reference sequence, which is the part of the genomic reference sequence that is converted to messenger RNA (i.e., after the introns are removed). The transcript reference sequence ID may be reporting using various coding systems including NCBI's RefSeq ("NM_..."), Ensembl ("ENST..."), and LRG ("LRG..." plus "t1" to indicate transcript).
statusACTIVE

Fully-Specified Name

componentTranscript reference sequence identifier
propertyID  =  Identifier
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
method

Additional Names

short nameTranscript ref sequence ID

Basic Attributes

classHL7.GENETICS
type1  Laboratory
order vs. observationObservation

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

Member of these Panels

81250-3Discrete genetic variant panel
81250-3Discrete genetic variant panel
81250-3Discrete genetic variant panel
77313-5DNA analysis discrete sequence variation basic associated observations panel - Blood or Tissue by Molecular genetics method
55208-3DNA analysis discrete sequence variation panel
53042-8DNA marker assessed panel
53044-4DNA marker identified panel
53044-4DNA marker identified panel
53044-4DNA marker identified panel
53044-4DNA marker identified panel
78046-0Pharmacogenomic analysis basic associated observations panel - Blood or Tissue

History/Usage

test rank14335 of 2000 most commonly performed tests by labs in USA
first released
last updated2.73
last change typeMIN  - change to field other than name

Related Names

Blood
Genetic
Genetics
Genomic
Heredity
Heritable
HL7.GENETICS
Ident
Identifier
Inherited
MOLPATH.GENERAL
Nominal
Point in time
Random
Ref Sequence
RefSeq
Tissue
Tissue, unspecified
Transcript ref sequence ID
WB
Whole blood
Whole blood or Tissue

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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