Canonical Allele Identifier: CA767393331

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27412596A>T , CM000664.2:g.27412596A>T	GRCh38
NC_000002.11:g.27635463A>T , CM000664.1:g.27635463A>T	GRCh37
NC_000002.10:g.27488967A>T	NCBI36