Canonical Allele Identifier: CA218673744

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20334898G>C , CM000673.2:g.20334898G>C	GRCh38
NC_000011.9:g.20356444G>C , CM000673.1:g.20356444G>C	GRCh37
NC_000011.8:g.20313020G>C	NCBI36