Canonical Allele Identifier: CA382649849

Gene: DRD2

Linked Data

• dbSNP Id: rs1292384569
• gnomAD v2: 11-113283379-A-G
• gnomAD v4: 11-113412657-A-G
• MyVariant Identifiers: chr11:g.113283379A>G (hg19) ; chr11:g.113412657A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412657A>G , CM000673.2:g.113412657A>G	GRCh38
NC_000011.9:g.113283379A>G , CM000673.1:g.113283379A>G	GRCh37
NC_000011.8:g.112788589A>G	NCBI36
NG_008841.1:g.67623T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1037T>C MANE Select	ENSP00000354859.3:p.Met346Thr
ENST00000346454.7:c.950T>C	ENSP00000278597.5:p.Met317Thr
ENST00000362072.7:c.1037T>C	ENSP00000354859.3:p.Met346Thr
ENST00000538967.5:c.1043T>C	ENSP00000438215.1:p.Met348Thr
ENST00000542968.5:c.1037T>C	ENSP00000442172.1:p.Met346Thr
ENST00000544518.5:c.1034T>C	ENSP00000441068.1:p.Met345Thr
NM_000795.3:c.1037T>C	NP_000786.1:p.Met346Thr
NM_016574.3:c.950T>C	NP_057658.2:p.Met317Thr
XM_017017296.2:c.1037T>C	XP_016872785.1:p.Met346Thr
NM_000795.4:c.1037T>C MANE Select	NP_000786.1:p.Met346Thr
NM_016574.4:c.950T>C	NP_057658.2:p.Met317Thr