Canonical Allele Identifier: CA837112709

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26143169A>G , CM000669.2:g.26143169A>G	GRCh38
NC_000007.13:g.26182789A>G , CM000669.1:g.26182789A>G	GRCh37
NC_000007.12:g.26149314A>G	NCBI36