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Preferred Name

Transcript Variant
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C185299
code

C185299
DEFINITION

Any change in the nucleotide sequence of an mRNA transcript, includes splicing variants and nucleotide mutations identified in a transcript.
FULL_SYN

Transcript Variant

Transcript Variation
label

Transcript Variant
NCI_META_CUI

CL1773567
Preferred_Name

Transcript Variant
prefixIRI

Thesaurus:C185299
prefLabel

Transcript Variant
Semantic_Type

Cell or Molecular Dysfunction
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97928
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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/SO_0001576 Sequence Types and Features Ontology / 序列类型和特征本体 LOOM
http://purl.obolibrary.org/obo/SO_0001576 Human Disease Ontology / 人类疾病本体 LOOM