Canonical Allele Identifier: CA382650267
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412757G>T , CM000673.2:g.113412757G>T GRCh38
NC_000011.9:g.113283479G>T , CM000673.1:g.113283479G>T GRCh37
NC_000011.8:g.112788689G>T NCBI36
NG_008841.1:g.67523C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.937C>A MANE Select ENSP00000354859.3:p.His313Asn
ENST00000346454.7:c.850C>A ENSP00000278597.5:p.His284Asn
ENST00000362072.7:c.937C>A ENSP00000354859.3:p.His313Asn
ENST00000538967.5:c.943C>A ENSP00000438215.1:p.His315Asn
ENST00000542968.5:c.937C>A ENSP00000442172.1:p.His313Asn
ENST00000544518.5:c.934C>A ENSP00000441068.1:p.His312Asn
NM_000795.3:c.937C>A NP_000786.1:p.His313Asn
NM_016574.3:c.850C>A NP_057658.2:p.His284Asn
XM_017017296.2:c.937C>A XP_016872785.1:p.His313Asn
NM_000795.4:c.937C>A MANE Select NP_000786.1:p.His313Asn
NM_016574.4:c.850C>A NP_057658.2:p.His284Asn