Canonical Allele Identifier: CA672352942

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118274971C>A , CM000673.2:g.118274971C>A	GRCh38
NC_000011.9:g.118145686C>A , CM000673.1:g.118145686C>A	GRCh37
NC_000011.8:g.117650896C>A	NCBI36