Canonical Allele Identifier: CA382650290
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412763A>T , CM000673.2:g.113412763A>T GRCh38
NC_000011.9:g.113283485A>T , CM000673.1:g.113283485A>T GRCh37
NC_000011.8:g.112788695A>T NCBI36
NG_008841.1:g.67517T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.931T>A MANE Select ENSP00000354859.3:p.Ser311Thr
ENST00000346454.7:c.844T>A ENSP00000278597.5:p.Ser282Thr
ENST00000362072.7:c.931T>A ENSP00000354859.3:p.Ser311Thr
ENST00000538967.5:c.937T>A ENSP00000438215.1:p.Ser313Thr
ENST00000542968.5:c.931T>A ENSP00000442172.1:p.Ser311Thr
ENST00000544518.5:c.928T>A ENSP00000441068.1:p.Ser310Thr
NM_000795.3:c.931T>A NP_000786.1:p.Ser311Thr
NM_016574.3:c.844T>A NP_057658.2:p.Ser282Thr
XM_017017296.2:c.931T>A XP_016872785.1:p.Ser311Thr
NM_000795.4:c.931T>A MANE Select NP_000786.1:p.Ser311Thr
NM_016574.4:c.844T>A NP_057658.2:p.Ser282Thr