Canonical Allele Identifier: CA804313168

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.135990901A>T , CM000667.2:g.135990901A>T	GRCh38
NC_000005.9:g.135326590A>T , CM000667.1:g.135326590A>T	GRCh37
NC_000005.8:g.135354489A>T	NCBI36