Canonical Allele Identifier: CA2001167067
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410611G= , CM000673.2:g.113410611G= GRCh38
NC_000011.9:g.113281333G= , CM000673.1:g.113281333G= GRCh37
NC_000011.8:g.112786543G= NCBI36
NG_008841.1:g.69669C=

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.*116C= MANE Select ENSP00000354859.3:n.*116C=
ENST00000346454.7:c.*116C= ENSP00000278597.5:n.*116C=
ENST00000362072.7:c.*116C= ENSP00000354859.3:n.*116C=
ENST00000538967.5:c.1454C= ENSP00000438215.1:n.1454C=
ENST00000542968.5:c.*116C= ENSP00000442172.1:n.*116C=
ENST00000544518.5:c.*116C= ENSP00000441068.1:n.*116C=
NM_000795.3:c.*116C= NP_000786.1:n.*116C=
NM_016574.3:c.*116C= NP_057658.2:n.*116C=
XM_017017296.2:c.*116C= XP_016872785.1:n.*116C=
NM_000795.4:c.*116C= MANE Select NP_000786.1:n.*116C=
NM_016574.4:c.*116C= NP_057658.2:n.*116C=