Canonical Allele Identifier: CA228624683

Gene: DRD2

Linked Data

• dbSNP Id: rs200147005
• gnomAD v2: 11-113281332-C-T
• gnomAD v3: 11-113410610-C-T
• gnomAD v4: 11-113410610-C-T
• MyVariant Identifiers: chr11:g.113281332C>T (hg19) ; chr11:g.113410610C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410610C>T , CM000673.2:g.113410610C>T	GRCh38
NC_000011.9:g.113281332C>T , CM000673.1:g.113281332C>T	GRCh37
NC_000011.8:g.112786542C>T	NCBI36
NG_008841.1:g.69670G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.*117G>A MANE Select	ENSP00000354859.3:n.*117G>A
ENST00000346454.7:c.*117G>A	ENSP00000278597.5:n.*117G>A
ENST00000362072.7:c.*117G>A	ENSP00000354859.3:n.*117G>A
ENST00000538967.5:c.1455G>A	ENSP00000438215.1:n.1455G>A
ENST00000542968.5:c.*117G>A	ENSP00000442172.1:n.*117G>A
ENST00000544518.5:c.*117G>A	ENSP00000441068.1:n.*117G>A
NM_000795.3:c.*117G>A	NP_000786.1:n.*117G>A
NM_016574.3:c.*117G>A	NP_057658.2:n.*117G>A
XM_017017296.2:c.*117G>A	XP_016872785.1:n.*117G>A
NM_000795.4:c.*117G>A MANE Select	NP_000786.1:n.*117G>A
NM_016574.4:c.*117G>A	NP_057658.2:n.*117G>A