Canonical Allele Identifier: CA799611125

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87854091T>A , CM000666.2:g.87854091T>A	GRCh38
NC_000004.11:g.88775243T>A , CM000666.1:g.88775243T>A	GRCh37
NC_000004.10:g.88994267T>A	NCBI36