Canonical Allele Identifier: CA780606697

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.55153893A>T , CM000680.2:g.55153893A>T	GRCh38
NC_000018.9:g.52821124A>T , CM000680.1:g.52821124A>T	GRCh37
NC_000018.8:g.50972122A>T	NCBI36