Canonical Allele Identifier: CA2001167955
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412643T= , CM000673.2:g.113412643T= GRCh38
NC_000011.9:g.113283365T= , CM000673.1:g.113283365T= GRCh37
NC_000011.8:g.112788575T= NCBI36
NG_008841.1:g.67637A=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.1051A= MANE Select ENSP00000354859.3:p.Thr351=
ENST00000346454.7:c.964A= ENSP00000278597.5:p.Thr322=
ENST00000362072.7:c.1051A= ENSP00000354859.3:p.Thr351=
ENST00000538967.5:c.1057A= ENSP00000438215.1:p.Thr353=
ENST00000542968.5:c.1051A= ENSP00000442172.1:p.Thr351=
ENST00000544518.5:c.1048A= ENSP00000441068.1:p.Thr350=
NM_000795.3:c.1051A= NP_000786.1:p.Thr351=
NM_016574.3:c.964A= NP_057658.2:p.Thr322=
XM_017017296.2:c.1051A= XP_016872785.1:p.Thr351=
NM_000795.4:c.1051A= MANE Select NP_000786.1:p.Thr351=
NM_016574.4:c.964A= NP_057658.2:p.Thr322=