Canonical Allele Identifier: CA203433
Gene: DRD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 198436
ClinVar RCV Id: RCV000179786
dbSNP Id: rs6277

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412737G>A , CM000673.2:g.113412737G>A GRCh38
NC_000011.9:g.113283459G>A , CM000673.1:g.113283459G>A GRCh37
NC_000011.8:g.112788669G>A NCBI36
NG_008841.1:g.67543C>T

Transcript Alleles

HGVS Amino-acid change
NM_000795.3:c.957C>T NP_000786.1:p.Pro319=
NM_016574.3:c.870C>T NP_057658.2:p.Pro290=
XM_017017296.2:c.957C>T XP_016872785.1:p.Pro319=
NM_000795.4:c.957C>T MANE Select NP_000786.1:p.Pro319=
NM_016574.4:c.870C>T NP_057658.2:p.Pro290=
ENST00000346454.7:c.870C>T ENSP00000278597.5:p.Pro290=
ENST00000362072.7:c.957C>T ENSP00000354859.3:p.Pro319=
ENST00000538967.5:n.963C>T ENSP00000438215.1:p.Pro321=
ENST00000542968.5:c.957C>T ENSP00000442172.1:p.Pro319=
ENST00000544518.5:c.954C>T ENSP00000441068.1:p.Pro318=