Canonical Allele Identifier: CA124924535
Gene:

Linked Data

ClinVar Variation Id: 664068
ClinVar RCV Id: RCV003537295
dbSNP Id: rs1050218356

Genomic Alleles

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