Canonical Allele Identifier: CA6281207

Gene: DRD2

Linked Data

• dbSNP Id: rs372849659
• ExAC: 11:113283397 A / G
• gnomAD v4: 11-113412675-A-G
• MyVariant Identifiers: chr11:g.113283397A>G (hg19) ; chr11:g.113412675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412675A>G , CM000673.2:g.113412675A>G	GRCh38
NC_000011.9:g.113283397A>G , CM000673.1:g.113283397A>G	GRCh37
NC_000011.8:g.112788607A>G	NCBI36
NG_008841.1:g.67605T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1019T>C MANE Select	ENSP00000354859.3:p.Ile340Thr
ENST00000346454.7:c.932T>C	ENSP00000278597.5:p.Ile311Thr
ENST00000362072.7:c.1019T>C	ENSP00000354859.3:p.Ile340Thr
ENST00000538967.5:c.1025T>C	ENSP00000438215.1:p.Ile342Thr
ENST00000542968.5:c.1019T>C	ENSP00000442172.1:p.Ile340Thr
ENST00000544518.5:c.1016T>C	ENSP00000441068.1:p.Ile339Thr
NM_000795.3:c.1019T>C	NP_000786.1:p.Ile340Thr
NM_016574.3:c.932T>C	NP_057658.2:p.Ile311Thr
XM_017017296.2:c.1019T>C	XP_016872785.1:p.Ile340Thr
NM_000795.4:c.1019T>C MANE Select	NP_000786.1:p.Ile340Thr
NM_016574.4:c.932T>C	NP_057658.2:p.Ile311Thr