Canonical Allele Identifier: CA477043197

Gene: DRD2

Linked Data

• ClinVar Variation Id: 1157468
• ClinVar RCV Id: RCV001500531
• dbSNP Id: rs909622147
• gnomAD v3: 11-113412752-A-G
• gnomAD v4: 11-113412752-A-G
• MyVariant Identifiers: chr11:g.113283474A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412752A>G , CM000673.2:g.113412752A>G	GRCh38
NC_000011.9:g.113283474A>G , CM000673.1:g.113283474A>G	GRCh37
NC_000011.8:g.112788684A>G	NCBI36
NG_008841.1:g.67528T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.942T>C MANE Select	ENSP00000354859.3:p.Gly314=
ENST00000346454.7:c.855T>C	ENSP00000278597.5:p.Gly285=
ENST00000362072.7:c.942T>C	ENSP00000354859.3:p.Gly314=
ENST00000538967.5:c.948T>C	ENSP00000438215.1:p.Gly316=
ENST00000542968.5:c.942T>C	ENSP00000442172.1:p.Gly314=
ENST00000544518.5:c.939T>C	ENSP00000441068.1:p.Gly313=
NM_000795.3:c.942T>C	NP_000786.1:p.Gly314=
NM_016574.3:c.855T>C	NP_057658.2:p.Gly285=
XM_017017296.2:c.942T>C	XP_016872785.1:p.Gly314=
NM_000795.4:c.942T>C MANE Select	NP_000786.1:p.Gly314=
NM_016574.4:c.855T>C	NP_057658.2:p.Gly285=