Canonical Allele Identifier: CA682820675

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102497908T>A , CM000674.2:g.102497908T>A	GRCh38
NC_000012.11:g.102891686T>A , CM000674.1:g.102891686T>A	GRCh37
NC_000012.10:g.101415816T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001749289.1:n.1952+14020T>A