Canonical Allele Identifier: CA382649820
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412650A>T , CM000673.2:g.113412650A>T GRCh38
NC_000011.9:g.113283372A>T , CM000673.1:g.113283372A>T GRCh37
NC_000011.8:g.112788582A>T NCBI36
NG_008841.1:g.67630T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.1044T>A MANE Select ENSP00000354859.3:p.Asn348Lys
ENST00000346454.7:c.957T>A ENSP00000278597.5:p.Asn319Lys
ENST00000362072.7:c.1044T>A ENSP00000354859.3:p.Asn348Lys
ENST00000538967.5:c.1050T>A ENSP00000438215.1:p.Asn350Lys
ENST00000542968.5:c.1044T>A ENSP00000442172.1:p.Asn348Lys
ENST00000544518.5:c.1041T>A ENSP00000441068.1:p.Asn347Lys
NM_000795.3:c.1044T>A NP_000786.1:p.Asn348Lys
NM_016574.3:c.957T>A NP_057658.2:p.Asn319Lys
XM_017017296.2:c.1044T>A XP_016872785.1:p.Asn348Lys
NM_000795.4:c.1044T>A MANE Select NP_000786.1:p.Asn348Lys
NM_016574.4:c.957T>A NP_057658.2:p.Asn319Lys