Canonical Allele Identifier: CA782638238

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.77160709C>A , CM000680.2:g.77160709C>A	GRCh38
NC_000018.9:g.74872665C>A , CM000680.1:g.74872665C>A	GRCh37
NC_000018.8:g.73001653C>A	NCBI36