Canonical Allele Identifier: CA2001168007
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412764C= , CM000673.2:g.113412764C= GRCh38
NC_000011.9:g.113283486C= , CM000673.1:g.113283486C= GRCh37
NC_000011.8:g.112788696C= NCBI36
NG_008841.1:g.67516G=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.930G= MANE Select ENSP00000354859.3:p.Pro310=
ENST00000346454.7:c.843G= ENSP00000278597.5:p.Pro281=
ENST00000362072.7:c.930G= ENSP00000354859.3:p.Pro310=
ENST00000538967.5:c.936G= ENSP00000438215.1:p.Pro312=
ENST00000542968.5:c.930G= ENSP00000442172.1:p.Pro310=
ENST00000544518.5:c.927G= ENSP00000441068.1:p.Pro309=
NM_000795.3:c.930G= NP_000786.1:p.Pro310=
NM_016574.3:c.843G= NP_057658.2:p.Pro281=
XM_017017296.2:c.930G= XP_016872785.1:p.Pro310=
NM_000795.4:c.930G= MANE Select NP_000786.1:p.Pro310=
NM_016574.4:c.843G= NP_057658.2:p.Pro281=