Canonical Allele Identifier: CA689072263

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4408974G>A , CM000674.2:g.4408974G>A	GRCh38
NC_000012.11:g.4518140G>A , CM000674.1:g.4518140G>A	GRCh37
NC_000012.10:g.4388401G>A	NCBI36