Canonical Allele Identifier: CA773296991

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.55680426T>A , CM000679.2:g.55680426T>A	GRCh38
NC_000017.10:g.53757787T>A , CM000679.1:g.53757787T>A	GRCh37
NC_000017.9:g.51112786T>A	NCBI36