Canonical Allele Identifier: CA671871989

Gene: DRD2

Linked Data

• dbSNP Id: rs1241253160
• gnomAD v3: 11-113420878-C-G
• gnomAD v4: 11-113420878-C-G
• MyVariant Identifiers: chr11:g.113291600C>G (hg19) ; chr11:g.113420878C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113420878C>G , CM000673.2:g.113420878C>G	GRCh38
NC_000011.9:g.113291600C>G , CM000673.1:g.113291600C>G	GRCh37
NC_000011.8:g.112796810C>G	NCBI36
NG_008841.1:g.59402G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.286-2742G>C MANE Select	ENSP00000354859.3:n.286-2742G>C
ENST00000346454.7:c.286-2742G>C	ENSP00000278597.5:n.286-2742G>C
ENST00000362072.7:c.286-2742G>C	ENSP00000354859.3:n.286-2742G>C
ENST00000535984.1:n.142-2742G>C
ENST00000538967.5:c.286-2742G>C	ENSP00000438215.1:n.286-2742G>C
ENST00000540600.5:n.351-2742G>C
ENST00000542968.5:c.286-2742G>C	ENSP00000442172.1:n.286-2742G>C
ENST00000543292.1:c.286-2742G>C	ENSP00000438419.1:n.286-2742G>C
ENST00000544518.5:c.290-2749G>C	ENSP00000441068.1:n.290-2749G>C
NM_000795.3:c.286-2742G>C	NP_000786.1:n.286-2742G>C
NM_016574.3:c.286-2742G>C	NP_057658.2:n.286-2742G>C
XM_017017296.2:c.286-2742G>C	XP_016872785.1:n.286-2742G>C
NM_000795.4:c.286-2742G>C MANE Select	NP_000786.1:n.286-2742G>C
NM_016574.4:c.286-2742G>C	NP_057658.2:n.286-2742G>C