Canonical Allele Identifier: CA124924643
Gene:

Linked Data

ClinVar Variation Id: 469877
ClinVar RCV Id: RCV003537057
dbSNP Id: rs372923973

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707418A>C , CM000667.2:g.112707418A>C GRCh38
NC_000005.9:g.112043115A>C , CM000667.1:g.112043115A>C GRCh37
NC_000005.8:g.112071014A>C NCBI36
NG_008481.4:g.19898A>C , LRG_130:g.19898A>C