Canonical Allele Identifier: CA884629922

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.101472921G>C , CM000663.2:g.101472921G>C	GRCh38
NC_000001.10:g.101938477G>C , CM000663.1:g.101938477G>C	GRCh37
NC_000001.9:g.101711065G>C	NCBI36