Canonical Allele Identifier: CA228625638

Gene: DRD2

Linked Data

• dbSNP Id: rs201256011
• gnomAD v2: 11-113283396-G-T
• gnomAD v4: 11-113412674-G-T
• MyVariant Identifiers: chr11:g.113283396G>T (hg19) ; chr11:g.113412674G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412674G>T , CM000673.2:g.113412674G>T	GRCh38
NC_000011.9:g.113283396G>T , CM000673.1:g.113283396G>T	GRCh37
NC_000011.8:g.112788606G>T	NCBI36
NG_008841.1:g.67606C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1020C>A MANE Select	ENSP00000354859.3:p.Ile340=
ENST00000346454.7:c.933C>A	ENSP00000278597.5:p.Ile311=
ENST00000362072.7:c.1020C>A	ENSP00000354859.3:p.Ile340=
ENST00000538967.5:c.1026C>A	ENSP00000438215.1:p.Ile342=
ENST00000542968.5:c.1020C>A	ENSP00000442172.1:p.Ile340=
ENST00000544518.5:c.1017C>A	ENSP00000441068.1:p.Ile339=
NM_000795.3:c.1020C>A	NP_000786.1:p.Ile340=
NM_016574.3:c.933C>A	NP_057658.2:p.Ile311=
XM_017017296.2:c.1020C>A	XP_016872785.1:p.Ile340=
NM_000795.4:c.1020C>A MANE Select	NP_000786.1:p.Ile340=
NM_016574.4:c.933C>A	NP_057658.2:p.Ile311=