Canonical Allele Identifier: CA452310602

Gene: LINC01312 TARID

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133837662T>A , CM000668.2:g.133837662T>A	GRCh38
NC_000006.11:g.134158800T>A , CM000668.1:g.134158800T>A	GRCh37
NC_000006.10:g.134200493T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_027030.1:n.659T>A (LINC01312)
NR_109982.1:n.478+8215A>T (TARID)