Canonical Allele Identifier: CA667767311

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67920067T>A , CM000672.2:g.67920067T>A	GRCh38
NC_000010.10:g.69679824T>A , CM000672.1:g.69679824T>A	GRCh37
NC_000010.9:g.69349830T>A	NCBI36
NG_050664.1:g.40406T>A