Canonical Allele Identifier: CA6281133

Gene: DRD2

Linked Data

• dbSNP Id: rs199542111
• ExAC: 11:113281429 T / C
• gnomAD v2: 11-113281429-T-C
• gnomAD v3: 11-113410707-T-C
• gnomAD v4: 11-113410707-T-C
• MyVariant Identifiers: chr11:g.113281429T>C (hg19) ; chr11:g.113410707T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410707T>C , CM000673.2:g.113410707T>C	GRCh38
NC_000011.9:g.113281429T>C , CM000673.1:g.113281429T>C	GRCh37
NC_000011.8:g.112786639T>C	NCBI36
NG_008841.1:g.69573A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*20A>G MANE Select	ENSP00000354859.3:n.*20A>G
ENST00000346454.7:c.*20A>G	ENSP00000278597.5:n.*20A>G
ENST00000362072.7:c.*20A>G	ENSP00000354859.3:n.*20A>G
ENST00000538967.5:c.1358A>G	ENSP00000438215.1:n.1358A>G
ENST00000542968.5:c.*20A>G	ENSP00000442172.1:n.*20A>G
ENST00000544518.5:c.*20A>G	ENSP00000441068.1:n.*20A>G
NM_000795.3:c.*20A>G	NP_000786.1:n.*20A>G
NM_016574.3:c.*20A>G	NP_057658.2:n.*20A>G
XM_017017296.2:c.*20A>G	XP_016872785.1:n.*20A>G
NM_000795.4:c.*20A>G MANE Select	NP_000786.1:n.*20A>G
NM_016574.4:c.*20A>G	NP_057658.2:n.*20A>G