Canonical Allele Identifier: CA6281224
Gene: DRD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 256814
ClinVar RCV Id: RCV000242384
dbSNP Id: rs6275

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412755A>G , CM000673.2:g.113412755A>G GRCh38
NC_000011.9:g.113283477A>G , CM000673.1:g.113283477A>G GRCh37
NC_000011.8:g.112788687A>G NCBI36
NG_008841.1:g.67525T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.939T>C MANE Select ENSP00000354859.3:p.His313=
ENST00000346454.7:c.852T>C ENSP00000278597.5:p.His284=
ENST00000362072.7:c.939T>C ENSP00000354859.3:p.His313=
ENST00000538967.5:n.945T>C ENSP00000438215.1:p.His315=
ENST00000542968.5:c.939T>C ENSP00000442172.1:p.His313=
ENST00000544518.5:c.936T>C ENSP00000441068.1:p.His312=
NM_000795.3:c.939T>C NP_000786.1:p.His313=
NM_016574.3:c.852T>C NP_057658.2:p.His284=
XM_017017296.2:c.939T>C XP_016872785.1:p.His313=
NM_000795.4:c.939T>C MANE Select NP_000786.1:p.His313=
NM_016574.4:c.852T>C NP_057658.2:p.His284=