Canonical Allele Identifier: CA875667252

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.45874916G>A , CM000685.2:g.45874916G>A	GRCh38
NC_000023.10:g.45734351G>A , CM000685.1:g.45734351G>A	GRCh37
NC_000023.9:g.45619295G>A	NCBI36