Canonical Allele Identifier: CA13449567
Gene: DRD2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4648318

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113442667T>C , CM000673.2:g.113442667T>C GRCh38
NC_000011.9:g.113313389T>C , CM000673.1:g.113313389T>C GRCh37
NC_000011.8:g.112818599T>C NCBI36
NG_008841.1:g.37613A>G

Transcript Alleles

HGVS Amino-acid change
NM_000795.3:c.-31-17985A>G VV NP_000786.1:p.=
NM_016574.3:c.-31-17985A>G VV NP_057658.2:p.=
XM_017017296.2:c.-31-17985A>G XP_016872785.1:p.=
NM_000795.4:c.-31-17985A>G VV MANE Preferred NP_000786.1:p.=
ENST00000346454.7:c.-31-17985A>G ENSP00000278597.5:p.=
ENST00000362072.7:c.-31-17985A>G ENSP00000354859.3:p.=
ENST00000540600.5:n.35-17985A>G
ENST00000542616.1:c.-31-17985A>G ENSP00000441474.1:p.=
ENST00000543292.1:c.-32+4904A>G ENSP00000438419.1:p.=