Canonical Allele Identifier: CA1573442221
Gene:

Linked Data

ClinVar Variation Id: 1035644
ClinVar RCV Id: RCV003538707
dbSNP Id: rs1750553249

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707375_112707376delinsGC , CM000667.2:g.112707375_112707376delinsGC GRCh38
NC_000005.9:g.112043072_112043073delinsGC , CM000667.1:g.112043072_112043073delinsGC GRCh37
NC_000005.8:g.112070971_112070972delinsGC NCBI36
NG_008481.4:g.19855_19856delinsGC , LRG_130:g.19855_19856delinsGC