Canonical Allele Identifier: CA2001168005
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412762G= , CM000673.2:g.113412762G= GRCh38
NC_000011.9:g.113283484G= , CM000673.1:g.113283484G= GRCh37
NC_000011.8:g.112788694G= NCBI36
NG_008841.1:g.67518C=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.932C= MANE Select ENSP00000354859.3:p.Ser311=
ENST00000346454.7:c.845C= ENSP00000278597.5:p.Ser282=
ENST00000362072.7:c.932C= ENSP00000354859.3:p.Ser311=
ENST00000538967.5:c.938C= ENSP00000438215.1:p.Ser313=
ENST00000542968.5:c.932C= ENSP00000442172.1:p.Ser311=
ENST00000544518.5:c.929C= ENSP00000441068.1:p.Ser310=
NM_000795.3:c.932C= NP_000786.1:p.Ser311=
NM_016574.3:c.845C= NP_057658.2:p.Ser282=
XM_017017296.2:c.932C= XP_016872785.1:p.Ser311=
NM_000795.4:c.932C= MANE Select NP_000786.1:p.Ser311=
NM_016574.4:c.845C= NP_057658.2:p.Ser282=