Canonical Allele Identifier: CA2001167112
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410691G= , CM000673.2:g.113410691G= GRCh38
NC_000011.9:g.113281413G= , CM000673.1:g.113281413G= GRCh37
NC_000011.8:g.112786623G= NCBI36
NG_008841.1:g.69589C=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.*36C= MANE Select ENSP00000354859.3:n.*36C=
ENST00000346454.7:c.*36C= ENSP00000278597.5:n.*36C=
ENST00000362072.7:c.*36C= ENSP00000354859.3:n.*36C=
ENST00000538967.5:c.1374C= ENSP00000438215.1:n.1374C=
ENST00000542968.5:c.*36C= ENSP00000442172.1:n.*36C=
ENST00000544518.5:c.*36C= ENSP00000441068.1:n.*36C=
NM_000795.3:c.*36C= NP_000786.1:n.*36C=
NM_016574.3:c.*36C= NP_057658.2:n.*36C=
XM_017017296.2:c.*36C= XP_016872785.1:n.*36C=
NM_000795.4:c.*36C= MANE Select NP_000786.1:n.*36C=
NM_016574.4:c.*36C= NP_057658.2:n.*36C=