Canonical Allele Identifier: CA890143444

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160887174A>T , CM000663.2:g.160887174A>T	GRCh38
NC_000001.10:g.160856964A>T , CM000663.1:g.160856964A>T	GRCh37
NC_000001.9:g.159123588A>T	NCBI36