Canonical Allele Identifier: CA316558437

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54798000T>A , CM000682.2:g.54798000T>A	GRCh38
NC_000020.10:g.53414539T>A , CM000682.1:g.53414539T>A	GRCh37
NC_000020.9:g.52847946T>A	NCBI36