Canonical Allele Identifier: CA382650108
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412718C>T , CM000673.2:g.113412718C>T GRCh38
NC_000011.9:g.113283440C>T , CM000673.1:g.113283440C>T GRCh37
NC_000011.8:g.112788650C>T NCBI36
NG_008841.1:g.67562G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.976G>A MANE Select ENSP00000354859.3:p.Glu326Lys
ENST00000346454.7:c.889G>A ENSP00000278597.5:p.Glu297Lys
ENST00000362072.7:c.976G>A ENSP00000354859.3:p.Glu326Lys
ENST00000538967.5:c.982G>A ENSP00000438215.1:p.Glu328Lys
ENST00000542968.5:c.976G>A ENSP00000442172.1:p.Glu326Lys
ENST00000544518.5:c.973G>A ENSP00000441068.1:p.Glu325Lys
NM_000795.3:c.976G>A NP_000786.1:p.Glu326Lys
NM_016574.3:c.889G>A NP_057658.2:p.Glu297Lys
XM_017017296.2:c.976G>A XP_016872785.1:p.Glu326Lys
NM_000795.4:c.976G>A MANE Select NP_000786.1:p.Glu326Lys
NM_016574.4:c.889G>A NP_057658.2:p.Glu297Lys