Canonical Allele Identifier: CA228625634

Gene: DRD2

Linked Data

• ClinVar Variation Id: 2726405
• ClinVar RCV Id: RCV003587186
• dbSNP Id: rs1054271642
• gnomAD v2: 11-113283393-A-G
• gnomAD v3: 11-113412671-A-G
• gnomAD v4: 11-113412671-A-G
• MyVariant Identifiers: chr11:g.113283393A>G (hg19) ; chr11:g.113412671A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412671A>G , CM000673.2:g.113412671A>G	GRCh38
NC_000011.9:g.113283393A>G , CM000673.1:g.113283393A>G	GRCh37
NC_000011.8:g.112788603A>G	NCBI36
NG_008841.1:g.67609T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1023T>C MANE Select	ENSP00000354859.3:p.Phe341=
ENST00000346454.7:c.936T>C	ENSP00000278597.5:p.Phe312=
ENST00000362072.7:c.1023T>C	ENSP00000354859.3:p.Phe341=
ENST00000538967.5:c.1029T>C	ENSP00000438215.1:p.Phe343=
ENST00000542968.5:c.1023T>C	ENSP00000442172.1:p.Phe341=
ENST00000544518.5:c.1020T>C	ENSP00000441068.1:p.Phe340=
NM_000795.3:c.1023T>C	NP_000786.1:p.Phe341=
NM_016574.3:c.936T>C	NP_057658.2:p.Phe312=
XM_017017296.2:c.1023T>C	XP_016872785.1:p.Phe341=
NM_000795.4:c.1023T>C MANE Select	NP_000786.1:p.Phe341=
NM_016574.4:c.936T>C	NP_057658.2:p.Phe312=