Canonical Allele Identifier: CA130189275

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157603306G>A , CM000667.2:g.157603306G>A	GRCh38
NC_000005.9:g.157030314G>A , CM000667.1:g.157030314G>A	GRCh37
NC_000005.8:g.156962892G>A	NCBI36