Canonical Allele Identifier: CA799781106

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89843548C>A , CM000666.2:g.89843548C>A	GRCh38
NC_000004.11:g.90764699C>A , CM000666.1:g.90764699C>A	GRCh37
NC_000004.10:g.90983722C>A	NCBI36