Canonical Allele Identifier: CA662319620

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16257952C>A , CM000672.2:g.16257952C>A	GRCh38
NC_000010.10:g.16299951C>A , CM000672.1:g.16299951C>A	GRCh37
NC_000010.9:g.16339957C>A	NCBI36