Canonical Allele Identifier: CA744873631

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46111557C>G , CM000682.2:g.46111557C>G	GRCh38
NC_000020.10:g.44740196C>G , CM000682.1:g.44740196C>G	GRCh37
NC_000020.9:g.44173603C>G	NCBI36