Canonical Allele Identifier: CA2001152106
Community Standard Title: NM_000795.4(DRD2):c.-31-882G=
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113425564C= , CM000673.2:g.113425564C= GRCh38
NC_000011.9:g.113296286C= , CM000673.1:g.113296286C= GRCh37
NC_000011.8:g.112801496C= NCBI36
NG_008841.1:g.54716G=

Transcript Alleles

HGVS Amino-acid Change
NM_000795.4:c.-31-882G= MANE Select NP_000786.1:n.-31-882G=
ENST00000362072.8:c.-31-882G= MANE Select ENSP00000354859.3:n.-31-882G=
NM_000795.3:c.-31-882G= NP_000786.1:n.-31-882G=
NM_016574.3:c.-31-882G= NP_057658.2:n.-31-882G=
NM_016574.4:c.-31-882G= NP_057658.2:n.-31-882G=
ENST00000346454.7:c.-31-882G= ENSP00000278597.5:n.-31-882G=
ENST00000362072.7:c.-31-882G= ENSP00000354859.3:n.-31-882G=
ENST00000540600.5:n.35-882G=
ENST00000542616.1:c.-31-882G= ENSP00000441474.1:n.-31-882G=
ENST00000543292.1:c.-31-882G= ENSP00000438419.1:n.-31-882G=
XM_017017296.2:c.-31-882G= XP_016872785.1:n.-31-882G=