Canonical Allele Identifier: CA666387286

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.52815236G>A , CM000672.2:g.52815236G>A	GRCh38
NC_000010.10:g.54574996G>A , CM000672.1:g.54574996G>A	GRCh37
NC_000010.9:g.54245002G>A	NCBI36