Canonical Allele Identifier: CA2709742360

Gene:

Linked Data

• ClinVar Variation Id: 2799620
• ClinVar RCV Id: RCV003745885
• dbSNP Id: rs1050218356

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707343G>A , CM000667.2:g.112707343G>A	GRCh38
NC_000005.9:g.112043040G>A , CM000667.1:g.112043040G>A	GRCh37
NC_000005.8:g.112070939G>A	NCBI36
NG_008481.4:g.19823G>A , LRG_130:g.19823G>A