Canonical Allele Identifier: CA763586608

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.204251279T>A , CM000664.2:g.204251279T>A	GRCh38
NC_000002.11:g.205116002T>A , CM000664.1:g.205116002T>A	GRCh37
NC_000002.10:g.204824247T>A	NCBI36