Canonical Allele Identifier: CA6281131

Gene: DRD2

Linked Data

• dbSNP Id: rs757096560
• ExAC: 11:113281414 T / G
• gnomAD v2: 11-113281414-T-G
• gnomAD v4: 11-113410692-T-G
• MyVariant Identifiers: chr11:g.113281414T>G (hg19) ; chr11:g.113410692T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410692T>G , CM000673.2:g.113410692T>G	GRCh38
NC_000011.9:g.113281414T>G , CM000673.1:g.113281414T>G	GRCh37
NC_000011.8:g.112786624T>G	NCBI36
NG_008841.1:g.69588A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*35A>C MANE Select	ENSP00000354859.3:n.*35A>C
ENST00000346454.7:c.*35A>C	ENSP00000278597.5:n.*35A>C
ENST00000362072.7:c.*35A>C	ENSP00000354859.3:n.*35A>C
ENST00000538967.5:c.1373A>C	ENSP00000438215.1:n.1373A>C
ENST00000542968.5:c.*35A>C	ENSP00000442172.1:n.*35A>C
ENST00000544518.5:c.*35A>C	ENSP00000441068.1:n.*35A>C
NM_000795.3:c.*35A>C	NP_000786.1:n.*35A>C
NM_016574.3:c.*35A>C	NP_057658.2:n.*35A>C
XM_017017296.2:c.*35A>C	XP_016872785.1:n.*35A>C
NM_000795.4:c.*35A>C MANE Select	NP_000786.1:n.*35A>C
NM_016574.4:c.*35A>C	NP_057658.2:n.*35A>C