Canonical Allele Identifier: CA228636496

Gene: DRD2

Linked Data

• dbSNP Id: rs1006849319
• gnomAD v3: 11-113442671-T-C
• gnomAD v4: 11-113442671-T-C
• MyVariant Identifiers: chr11:g.113313393T>C (hg19) ; chr11:g.113442671T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442671T>C , CM000673.2:g.113442671T>C	GRCh38
NC_000011.9:g.113313393T>C , CM000673.1:g.113313393T>C	GRCh37
NC_000011.8:g.112818603T>C	NCBI36
NG_008841.1:g.37609A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-17989A>G MANE Select	ENSP00000354859.3:n.-31-17989A>G
ENST00000346454.7:c.-31-17989A>G	ENSP00000278597.5:n.-31-17989A>G
ENST00000362072.7:c.-31-17989A>G	ENSP00000354859.3:n.-31-17989A>G
ENST00000540600.5:n.35-17989A>G
ENST00000542616.1:c.-31-17989A>G	ENSP00000441474.1:n.-31-17989A>G
ENST00000543292.1:c.-32+4900A>G	ENSP00000438419.1:n.-32+4900A>G
NM_000795.3:c.-31-17989A>G	NP_000786.1:n.-31-17989A>G
NM_016574.3:c.-31-17989A>G	NP_057658.2:n.-31-17989A>G
XM_017017296.2:c.-31-17989A>G	XP_016872785.1:n.-31-17989A>G
NM_000795.4:c.-31-17989A>G MANE Select	NP_000786.1:n.-31-17989A>G
NM_016574.4:c.-31-17989A>G	NP_057658.2:n.-31-17989A>G