Canonical Allele Identifier: CA2001159758
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439582G= , CM000673.2:g.113439582G= GRCh38
NC_000011.9:g.113310304G= , CM000673.1:g.113310304G= GRCh37
NC_000011.8:g.112815514G= NCBI36
NG_008841.1:g.40698C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-31-14900C= MANE Select ENSP00000354859.3:n.-31-14900C=
ENST00000346454.7:c.-31-14900C= ENSP00000278597.5:n.-31-14900C=
ENST00000362072.7:c.-31-14900C= ENSP00000354859.3:n.-31-14900C=
ENST00000540600.5:n.35-14900C=
ENST00000542616.1:c.-31-14900C= ENSP00000441474.1:n.-31-14900C=
ENST00000543292.1:c.-32+7989C= ENSP00000438419.1:n.-32+7989C=
NM_000795.3:c.-31-14900C= NP_000786.1:n.-31-14900C=
NM_016574.3:c.-31-14900C= NP_057658.2:n.-31-14900C=
XM_017017296.2:c.-31-14900C= XP_016872785.1:n.-31-14900C=
NM_000795.4:c.-31-14900C= MANE Select NP_000786.1:n.-31-14900C=
NM_016574.4:c.-31-14900C= NP_057658.2:n.-31-14900C=