Canonical Allele Identifier: CA724821632

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82617112A>G , CM000678.2:g.82617112A>G	GRCh38
NC_000016.9:g.82650717A>G , CM000678.1:g.82650717A>G	GRCh37
NC_000016.8:g.81208218A>G	NCBI36