Canonical Allele Identifier: CA2001159487
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439107C= , CM000673.2:g.113439107C= GRCh38
NC_000011.9:g.113309829C= , CM000673.1:g.113309829C= GRCh37
NC_000011.8:g.112815039C= NCBI36
NG_008841.1:g.41173G=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-31-14425G= MANE Select ENSP00000354859.3:n.-31-14425G=
ENST00000346454.7:c.-31-14425G= ENSP00000278597.5:n.-31-14425G=
ENST00000362072.7:c.-31-14425G= ENSP00000354859.3:n.-31-14425G=
ENST00000540600.5:n.35-14425G=
ENST00000542616.1:c.-31-14425G= ENSP00000441474.1:n.-31-14425G=
ENST00000543292.1:c.-32+8464G= ENSP00000438419.1:n.-32+8464G=
NM_000795.3:c.-31-14425G= NP_000786.1:n.-31-14425G=
NM_016574.3:c.-31-14425G= NP_057658.2:n.-31-14425G=
XM_017017296.2:c.-31-14425G= XP_016872785.1:n.-31-14425G=
NM_000795.4:c.-31-14425G= MANE Select NP_000786.1:n.-31-14425G=
NM_016574.4:c.-31-14425G= NP_057658.2:n.-31-14425G=