Canonical Allele Identifier: CA699992902

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.64376290T>A , CM000675.2:g.64376290T>A	GRCh38
NC_000013.10:g.64950422T>A , CM000675.1:g.64950422T>A	GRCh37
NC_000013.9:g.63848423T>A	NCBI36