Canonical Allele Identifier: CA715611802

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74373281C>A , CM000677.2:g.74373281C>A	GRCh38
NC_000015.9:g.74665622C>A , CM000677.1:g.74665622C>A	GRCh37
NC_000015.8:g.72452675C>A	NCBI36