Canonical Allele Identifier: CA862568161

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551369T>A , CM000671.2:g.25551369T>A	GRCh38
NC_000009.11:g.25551367T>A , CM000671.1:g.25551367T>A	GRCh37
NC_000009.10:g.25541367T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-797A>T
XR_929525.2:n.674-797A>T