Canonical Allele Identifier: CA382650098

Gene: DRD2

Linked Data

• gnomAD v4: 11-113412716-C-G
• MyVariant Identifiers: chr11:g.113283438C>G (hg19) ; chr11:g.113412716C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412716C>G , CM000673.2:g.113412716C>G	GRCh38
NC_000011.9:g.113283438C>G , CM000673.1:g.113283438C>G	GRCh37
NC_000011.8:g.112788648C>G	NCBI36
NG_008841.1:g.67564G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.978G>C MANE Select	ENSP00000354859.3:p.Glu326Asp
ENST00000346454.7:c.891G>C	ENSP00000278597.5:p.Glu297Asp
ENST00000362072.7:c.978G>C	ENSP00000354859.3:p.Glu326Asp
ENST00000538967.5:c.984G>C	ENSP00000438215.1:p.Glu328Asp
ENST00000542968.5:c.978G>C	ENSP00000442172.1:p.Glu326Asp
ENST00000544518.5:c.975G>C	ENSP00000441068.1:p.Glu325Asp
NM_000795.3:c.978G>C	NP_000786.1:p.Glu326Asp
NM_016574.3:c.891G>C	NP_057658.2:p.Glu297Asp
XM_017017296.2:c.978G>C	XP_016872785.1:p.Glu326Asp
NM_000795.4:c.978G>C MANE Select	NP_000786.1:p.Glu326Asp
NM_016574.4:c.891G>C	NP_057658.2:p.Glu297Asp