Canonical Allele Identifier: CA696552750

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.22179954A>T , CM000675.2:g.22179954A>T	GRCh38
NC_000013.10:g.22754093A>T , CM000675.1:g.22754093A>T	GRCh37
NC_000013.9:g.21652093A>T	NCBI36