Canonical Allele Identifier: CA862130776

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21701433T>A , CM000671.2:g.21701433T>A	GRCh38
NC_000009.11:g.21701432T>A , CM000671.1:g.21701432T>A	GRCh37
NC_000009.10:g.21691432T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.384+1484A>T