Canonical Allele Identifier: CA2001167960
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412655G= , CM000673.2:g.113412655G= GRCh38
NC_000011.9:g.113283377G= , CM000673.1:g.113283377G= GRCh37
NC_000011.8:g.112788587G= NCBI36
NG_008841.1:g.67625C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1039C= MANE Select ENSP00000354859.3:p.Pro347=
ENST00000346454.7:c.952C= ENSP00000278597.5:p.Pro318=
ENST00000362072.7:c.1039C= ENSP00000354859.3:p.Pro347=
ENST00000538967.5:c.1045C= ENSP00000438215.1:p.Pro349=
ENST00000542968.5:c.1039C= ENSP00000442172.1:p.Pro347=
ENST00000544518.5:c.1036C= ENSP00000441068.1:p.Pro346=
NM_000795.3:c.1039C= NP_000786.1:p.Pro347=
NM_016574.3:c.952C= NP_057658.2:p.Pro318=
XM_017017296.2:c.1039C= XP_016872785.1:p.Pro347=
NM_000795.4:c.1039C= MANE Select NP_000786.1:p.Pro347=
NM_016574.4:c.952C= NP_057658.2:p.Pro318=