Canonical Allele Identifier: CA890180203

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161302651A>C , CM000663.2:g.161302651A>C	GRCh38
NC_000001.10:g.161272441A>C , CM000663.1:g.161272441A>C	GRCh37
NC_000001.9:g.159539065A>C	NCBI36