Canonical Allele Identifier: CA696584842

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.22654552C>T , CM000675.2:g.22654552C>T	GRCh38
NC_000013.10:g.23228691C>T , CM000675.1:g.23228691C>T	GRCh37
NC_000013.9:g.22126691C>T	NCBI36