Canonical Allele Identifier: CA2001169001
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414865C= , CM000673.2:g.113414865C= GRCh38
NC_000011.9:g.113285587C= , CM000673.1:g.113285587C= GRCh37
NC_000011.8:g.112790797C= NCBI36
NG_008841.1:g.65415G=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.724-404G= MANE Select ENSP00000354859.3:n.724-404G=
ENST00000346454.7:c.723+556G= ENSP00000278597.5:n.723+556G=
ENST00000362072.7:c.724-404G= ENSP00000354859.3:n.724-404G=
ENST00000535984.1:n.443-404G=
ENST00000538967.5:c.724-404G= ENSP00000438215.1:n.724-404G=
ENST00000540600.5:n.789-404G=
ENST00000542968.5:c.724-404G= ENSP00000442172.1:n.724-404G=
ENST00000544518.5:c.721-404G= ENSP00000441068.1:n.721-404G=
NM_000795.3:c.724-404G= NP_000786.1:n.724-404G=
NM_016574.3:c.723+556G= NP_057658.2:n.723+556G=
XM_017017296.2:c.724-404G= XP_016872785.1:n.724-404G=
NM_000795.4:c.724-404G= MANE Select NP_000786.1:n.724-404G=
NM_016574.4:c.723+556G= NP_057658.2:n.723+556G=