Canonical Allele Identifier: CA2001167954
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412640G= , CM000673.2:g.113412640G= GRCh38
NC_000011.9:g.113283362G= , CM000673.1:g.113283362G= GRCh37
NC_000011.8:g.112788572G= NCBI36
NG_008841.1:g.67640C=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.1054C= MANE Select ENSP00000354859.3:p.Arg352=
ENST00000346454.7:c.967C= ENSP00000278597.5:p.Arg323=
ENST00000362072.7:c.1054C= ENSP00000354859.3:p.Arg352=
ENST00000538967.5:c.1060C= ENSP00000438215.1:p.Arg354=
ENST00000542968.5:c.1054C= ENSP00000442172.1:p.Arg352=
ENST00000544518.5:c.1051C= ENSP00000441068.1:p.Arg351=
NM_000795.3:c.1054C= NP_000786.1:p.Arg352=
NM_016574.3:c.967C= NP_057658.2:p.Arg323=
XM_017017296.2:c.1054C= XP_016872785.1:p.Arg352=
NM_000795.4:c.1054C= MANE Select NP_000786.1:p.Arg352=
NM_016574.4:c.967C= NP_057658.2:p.Arg323=