Canonical Allele Identifier: CA382649859

Gene: DRD2

Linked Data

• dbSNP Id: rs2138156450
• COSMIC: COSM6067311 ; COSM6067312
• MyVariant Identifiers: chr11:g.113283382G>T (hg19) ; chr11:g.113412660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412660G>T , CM000673.2:g.113412660G>T	GRCh38
NC_000011.9:g.113283382G>T , CM000673.1:g.113283382G>T	GRCh37
NC_000011.8:g.112788592G>T	NCBI36
NG_008841.1:g.67620C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1034C>A MANE Select	ENSP00000354859.3:p.Thr345Asn
ENST00000346454.7:c.947C>A	ENSP00000278597.5:p.Thr316Asn
ENST00000362072.7:c.1034C>A	ENSP00000354859.3:p.Thr345Asn
ENST00000538967.5:c.1040C>A	ENSP00000438215.1:p.Thr347Asn
ENST00000542968.5:c.1034C>A	ENSP00000442172.1:p.Thr345Asn
ENST00000544518.5:c.1031C>A	ENSP00000441068.1:p.Thr344Asn
NM_000795.3:c.1034C>A	NP_000786.1:p.Thr345Asn
NM_016574.3:c.947C>A	NP_057658.2:p.Thr316Asn
XM_017017296.2:c.1034C>A	XP_016872785.1:p.Thr345Asn
NM_000795.4:c.1034C>A MANE Select	NP_000786.1:p.Thr345Asn
NM_016574.4:c.947C>A	NP_057658.2:p.Thr316Asn