Canonical Allele Identifier: CA2001167086
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410650C= , CM000673.2:g.113410650C= GRCh38
NC_000011.9:g.113281372C= , CM000673.1:g.113281372C= GRCh37
NC_000011.8:g.112786582C= NCBI36
NG_008841.1:g.69630G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*77G= MANE Select ENSP00000354859.3:n.*77G=
ENST00000346454.7:c.*77G= ENSP00000278597.5:n.*77G=
ENST00000362072.7:c.*77G= ENSP00000354859.3:n.*77G=
ENST00000538967.5:c.1415G= ENSP00000438215.1:n.1415G=
ENST00000542968.5:c.*77G= ENSP00000442172.1:n.*77G=
ENST00000544518.5:c.*77G= ENSP00000441068.1:n.*77G=
NM_000795.3:c.*77G= NP_000786.1:n.*77G=
NM_016574.3:c.*77G= NP_057658.2:n.*77G=
XM_017017296.2:c.*77G= XP_016872785.1:n.*77G=
NM_000795.4:c.*77G= MANE Select NP_000786.1:n.*77G=
NM_016574.4:c.*77G= NP_057658.2:n.*77G=