Canonical Allele Identifier: CA477043076

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283360C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412638C>G , CM000673.2:g.113412638C>G	GRCh38
NC_000011.9:g.113283360C>G , CM000673.1:g.113283360C>G	GRCh37
NC_000011.8:g.112788570C>G	NCBI36
NG_008841.1:g.67642G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1056G>C MANE Select	ENSP00000354859.3:p.Arg352=
ENST00000346454.7:c.969G>C	ENSP00000278597.5:p.Arg323=
ENST00000362072.7:c.1056G>C	ENSP00000354859.3:p.Arg352=
ENST00000538967.5:c.1062G>C	ENSP00000438215.1:p.Arg354=
ENST00000542968.5:c.1056G>C	ENSP00000442172.1:p.Arg352=
ENST00000544518.5:c.1053G>C	ENSP00000441068.1:p.Arg351=
NM_000795.3:c.1056G>C	NP_000786.1:p.Arg352=
NM_016574.3:c.969G>C	NP_057658.2:p.Arg323=
XM_017017296.2:c.1056G>C	XP_016872785.1:p.Arg352=
NM_000795.4:c.1056G>C MANE Select	NP_000786.1:p.Arg352=
NM_016574.4:c.969G>C	NP_057658.2:p.Arg323=