Canonical Allele Identifier: CA228631686
Gene: DRD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1236510
dbSNP Id: rs1799732

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113475530dup , CM000673.2:g.113475530dup GRCh38
NC_000011.9:g.113346252dup , CM000673.1:g.113346252dup GRCh37
NC_000011.8:g.112851462dup NCBI36
NG_008841.1:g.4750dup

Transcript Alleles

HGVS Amino-acid change
ENST00000540600.5:n.34+128dup
XR_948024.2:n.912dup