Canonical Allele Identifier: CA867218790

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.78695764A>G , CM000671.2:g.78695764A>G	GRCh38
NC_000009.11:g.81310680A>G , CM000671.1:g.81310680A>G	GRCh37
NC_000009.10:g.80500500A>G	NCBI36