Canonical Allele Identifier: CA1573442303
Gene:

Linked Data

ClinVar Variation Id: 1044099
ClinVar RCV Id: RCV003538717
dbSNP Id: rs1313658633

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707442C>G , CM000667.2:g.112707442C>G GRCh38
NC_000005.9:g.112043139C>G , CM000667.1:g.112043139C>G GRCh37
NC_000005.8:g.112071038C>G NCBI36
NG_008481.4:g.19922C>G , LRG_130:g.19922C>G