Canonical Allele Identifier: CA382650342

Gene: DRD2

Linked Data

• dbSNP Id: rs1373591057
• gnomAD v3: 11-113412778-T-G
• gnomAD v4: 11-113412778-T-G
• MyVariant Identifiers: chr11:g.113283500T>G (hg19) ; chr11:g.113412778T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412778T>G , CM000673.2:g.113412778T>G	GRCh38
NC_000011.9:g.113283500T>G , CM000673.1:g.113283500T>G	GRCh37
NC_000011.8:g.112788710T>G	NCBI36
NG_008841.1:g.67502A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.916A>C MANE Select	ENSP00000354859.3:p.Thr306Pro
ENST00000346454.7:c.829A>C	ENSP00000278597.5:p.Thr277Pro
ENST00000362072.7:c.916A>C	ENSP00000354859.3:p.Thr306Pro
ENST00000538967.5:c.922A>C	ENSP00000438215.1:p.Thr308Pro
ENST00000542968.5:c.916A>C	ENSP00000442172.1:p.Thr306Pro
ENST00000544518.5:c.913A>C	ENSP00000441068.1:p.Thr305Pro
NM_000795.3:c.916A>C	NP_000786.1:p.Thr306Pro
NM_016574.3:c.829A>C	NP_057658.2:p.Thr277Pro
XM_017017296.2:c.916A>C	XP_016872785.1:p.Thr306Pro
NM_000795.4:c.916A>C MANE Select	NP_000786.1:p.Thr306Pro
NM_016574.4:c.829A>C	NP_057658.2:p.Thr277Pro