Canonical Allele Identifier: CA902378391

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169765066G>A , CM000665.2:g.169765066G>A	GRCh38
NC_000003.11:g.169482854G>A , CM000665.1:g.169482854G>A	GRCh37
NC_000003.10:g.170965548G>A	NCBI36
NG_016363.1:g.4995C>T , LRG_347:g.4995C>T