Canonical Allele Identifier: CA2001183716
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113464537A>C , CM000673.2:g.113464537A>C GRCh38
NC_000011.9:g.113335259A>C , CM000673.1:g.113335259A>C GRCh37
NC_000011.8:g.112840469A>C NCBI36
NG_008841.1:g.15743T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-32+10539T>G MANE Select ENSP00000354859.3:n.-32+10539T>G
ENST00000346454.7:c.-32+10539T>G ENSP00000278597.5:n.-32+10539T>G
ENST00000362072.7:c.-32+10539T>G ENSP00000354859.3:n.-32+10539T>G
ENST00000540600.5:n.34+11121T>G
ENST00000542616.1:c.-32+9693T>G ENSP00000441474.1:n.-32+9693T>G
NM_000795.3:c.-32+10539T>G NP_000786.1:n.-32+10539T>G
NM_016574.3:c.-32+10539T>G NP_057658.2:n.-32+10539T>G
XM_017017296.2:c.-32+9693T>G XP_016872785.1:n.-32+9693T>G
NM_000795.4:c.-32+10539T>G MANE Select NP_000786.1:n.-32+10539T>G
NM_016574.4:c.-32+10539T>G NP_057658.2:n.-32+10539T>G