Canonical Allele Identifier: CA690225692

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56810376G>A , CM000674.2:g.56810376G>A	GRCh38
NC_000012.11:g.57204160G>A , CM000674.1:g.57204160G>A	GRCh37
NC_000012.10:g.55490427G>A	NCBI36