Canonical Allele Identifier: CA862229711

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22134150G>A , CM000671.2:g.22134150G>A	GRCh38
NC_000009.11:g.22134149G>A , CM000671.1:g.22134149G>A	GRCh37
NC_000009.10:g.22124149G>A	NCBI36