Canonical Allele Identifier: CA477043168

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283447G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412725G>C , CM000673.2:g.113412725G>C	GRCh38
NC_000011.9:g.113283447G>C , CM000673.1:g.113283447G>C	GRCh37
NC_000011.8:g.112788657G>C	NCBI36
NG_008841.1:g.67555C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.969C>G MANE Select	ENSP00000354859.3:p.Ala323=
ENST00000346454.7:c.882C>G	ENSP00000278597.5:p.Ala294=
ENST00000362072.7:c.969C>G	ENSP00000354859.3:p.Ala323=
ENST00000538967.5:c.975C>G	ENSP00000438215.1:p.Ala325=
ENST00000542968.5:c.969C>G	ENSP00000442172.1:p.Ala323=
ENST00000544518.5:c.966C>G	ENSP00000441068.1:p.Ala322=
NM_000795.3:c.969C>G	NP_000786.1:p.Ala323=
NM_016574.3:c.882C>G	NP_057658.2:p.Ala294=
XM_017017296.2:c.969C>G	XP_016872785.1:p.Ala323=
NM_000795.4:c.969C>G MANE Select	NP_000786.1:p.Ala323=
NM_016574.4:c.882C>G	NP_057658.2:p.Ala294=