Canonical Allele Identifier: CA791661159

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.179363660T>A , CM000666.2:g.179363660T>A	GRCh38
NC_000004.11:g.180284814T>A , CM000666.1:g.180284814T>A	GRCh37
NC_000004.10:g.180521808T>A	NCBI36