Transcript reference sequence identifier:ID:Pt:Bld/Tiss:Nom:

Preferred Label : Transcript reference sequence identifier:ID:Pt:Bld/Tiss:Nom:;

LOINC status : ACTIVE;

LOINC display name : Transcript reference sequence Nom (Bld/Tiss) [ID];

LOINC long common name : Transcript reference sequence [ID];

LOINC short name : Transcript ref sequence ID;

LOINC description : This 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).;

Details

Origin ID

51958-7;

UMLS CUI

C2360721;

Has component
- Identifier [LOINC component]
- Reference sequence [LOINC component]
- Transcript reference sequence identifier [LOINC component]
Has property
- Identifier [LOINC Property]
Has scale
- Nom [LOINC scale]
Has system
- Blood [LOINC System]
- Blood or Tissue [LOINC System]
- Tissue and Smears [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- DNA analysis discrete sequence variation basic associated observations panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- DNA analysis discrete sequence variation panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- DNA marker assessed panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- DNA marker identified panel:-:Pt:Bld/Tiss:-:Molgen [LOINC code]
- Pharmacogenomic analysis basic associated observations panel:-:Pt:Bld/Tiss:-: [LOINC code]
- Simple variant panel:-:Pt:^Patient:-: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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