Canonical Allele Identifier: CA2001161843
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113442632G= , CM000673.2:g.113442632G= GRCh38
NC_000011.9:g.113313354G= , CM000673.1:g.113313354G= GRCh37
NC_000011.8:g.112818564G= NCBI36
NG_008841.1:g.37648C=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-31-17950C= MANE Select ENSP00000354859.3:n.-31-17950C=
ENST00000346454.7:c.-31-17950C= ENSP00000278597.5:n.-31-17950C=
ENST00000362072.7:c.-31-17950C= ENSP00000354859.3:n.-31-17950C=
ENST00000540600.5:n.35-17950C=
ENST00000542616.1:c.-31-17950C= ENSP00000441474.1:n.-31-17950C=
ENST00000543292.1:c.-32+4939C= ENSP00000438419.1:n.-32+4939C=
NM_000795.3:c.-31-17950C= NP_000786.1:n.-31-17950C=
NM_016574.3:c.-31-17950C= NP_057658.2:n.-31-17950C=
XM_017017296.2:c.-31-17950C= XP_016872785.1:n.-31-17950C=
NM_000795.4:c.-31-17950C= MANE Select NP_000786.1:n.-31-17950C=
NM_016574.4:c.-31-17950C= NP_057658.2:n.-31-17950C=