Canonical Allele Identifier: CA837112703

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26143140G>A , CM000669.2:g.26143140G>A	GRCh38
NC_000007.13:g.26182760G>A , CM000669.1:g.26182760G>A	GRCh37
NC_000007.12:g.26149285G>A	NCBI36