Canonical Allele Identifier: CA228625670

Gene: DRD2

Linked Data

• dbSNP Id: rs991658667
• gnomAD v3: 11-113412756-T-C
• gnomAD v4: 11-113412756-T-C
• MyVariant Identifiers: chr11:g.113283478T>C (hg19) ; chr11:g.113412756T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412756T>C , CM000673.2:g.113412756T>C	GRCh38
NC_000011.9:g.113283478T>C , CM000673.1:g.113283478T>C	GRCh37
NC_000011.8:g.112788688T>C	NCBI36
NG_008841.1:g.67524A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.938A>G MANE Select	ENSP00000354859.3:p.His313Arg
ENST00000346454.7:c.851A>G	ENSP00000278597.5:p.His284Arg
ENST00000362072.7:c.938A>G	ENSP00000354859.3:p.His313Arg
ENST00000538967.5:c.944A>G	ENSP00000438215.1:p.His315Arg
ENST00000542968.5:c.938A>G	ENSP00000442172.1:p.His313Arg
ENST00000544518.5:c.935A>G	ENSP00000441068.1:p.His312Arg
NM_000795.3:c.938A>G	NP_000786.1:p.His313Arg
NM_016574.3:c.851A>G	NP_057658.2:p.His284Arg
XM_017017296.2:c.938A>G	XP_016872785.1:p.His313Arg
NM_000795.4:c.938A>G MANE Select	NP_000786.1:p.His313Arg
NM_016574.4:c.851A>G	NP_057658.2:p.His284Arg