Canonical Allele Identifier: CA667892826

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69180045G>T , CM000672.2:g.69180045G>T	GRCh38
NC_000010.10:g.70939801G>T , CM000672.1:g.70939801G>T	GRCh37
NC_000010.9:g.70609807G>T	NCBI36