Canonical Allele Identifier: CA1573442274
Gene:

Linked Data

ClinVar Variation Id: 1036983
ClinVar RCV Id: RCV003770894
dbSNP Id: rs1580995550

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707415C>G , CM000667.2:g.112707415C>G GRCh38
NC_000005.9:g.112043112C>G , CM000667.1:g.112043112C>G GRCh37
NC_000005.8:g.112071011C>G NCBI36
NG_008481.4:g.19895C>G , LRG_130:g.19895C>G