Canonical Allele Identifier: CA798209520

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72649596T>A , CM000666.2:g.72649596T>A	GRCh38
NC_000004.11:g.73515313T>A , CM000666.1:g.73515313T>A	GRCh37
NC_000004.10:g.73734177T>A	NCBI36