Canonical Allele Identifier: CA2001167088
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410652C= , CM000673.2:g.113410652C= GRCh38
NC_000011.9:g.113281374C= , CM000673.1:g.113281374C= GRCh37
NC_000011.8:g.112786584C= NCBI36
NG_008841.1:g.69628G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*75G= MANE Select ENSP00000354859.3:n.*75G=
ENST00000346454.7:c.*75G= ENSP00000278597.5:n.*75G=
ENST00000362072.7:c.*75G= ENSP00000354859.3:n.*75G=
ENST00000538967.5:c.1413G= ENSP00000438215.1:n.1413G=
ENST00000542968.5:c.*75G= ENSP00000442172.1:n.*75G=
ENST00000544518.5:c.*75G= ENSP00000441068.1:n.*75G=
NM_000795.3:c.*75G= NP_000786.1:n.*75G=
NM_016574.3:c.*75G= NP_057658.2:n.*75G=
XM_017017296.2:c.*75G= XP_016872785.1:n.*75G=
NM_000795.4:c.*75G= MANE Select NP_000786.1:n.*75G=
NM_016574.4:c.*75G= NP_057658.2:n.*75G=