Canonical Allele Identifier: CA890665314

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.166348577A>T , CM000663.2:g.166348577A>T	GRCh38
NC_000001.10:g.166317814A>T , CM000663.1:g.166317814A>T	GRCh37
NC_000001.9:g.164584438A>T	NCBI36