Canonical Allele Identifier: CA778162431

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.28479148T>A , CM000680.2:g.28479148T>A	GRCh38
NC_000018.9:g.26059112T>A , CM000680.1:g.26059112T>A	GRCh37
NC_000018.8:g.24313110T>A	NCBI36