Canonical Allele Identifier: CA382650255
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412755A>T , CM000673.2:g.113412755A>T GRCh38
NC_000011.9:g.113283477A>T , CM000673.1:g.113283477A>T GRCh37
NC_000011.8:g.112788687A>T NCBI36
NG_008841.1:g.67525T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.939T>A MANE Select ENSP00000354859.3:p.His313Gln
ENST00000346454.7:c.852T>A ENSP00000278597.5:p.His284Gln
ENST00000362072.7:c.939T>A ENSP00000354859.3:p.His313Gln
ENST00000538967.5:c.945T>A ENSP00000438215.1:p.His315Gln
ENST00000542968.5:c.939T>A ENSP00000442172.1:p.His313Gln
ENST00000544518.5:c.936T>A ENSP00000441068.1:p.His312Gln
NM_000795.3:c.939T>A NP_000786.1:p.His313Gln
NM_016574.3:c.852T>A NP_057658.2:p.His284Gln
XM_017017296.2:c.939T>A XP_016872785.1:p.His313Gln
NM_000795.4:c.939T>A MANE Select NP_000786.1:p.His313Gln
NM_016574.4:c.852T>A NP_057658.2:p.His284Gln