Canonical Allele Identifier: CA2001167154
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410797A= , CM000673.2:g.113410797A= GRCh38
NC_000011.9:g.113281519A= , CM000673.1:g.113281519A= GRCh37
NC_000011.8:g.112786729A= NCBI36
NG_008841.1:g.69483T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1262T= MANE Select ENSP00000354859.3:p.Val421=
ENST00000346454.7:c.1175T= ENSP00000278597.5:p.Val392=
ENST00000362072.7:c.1262T= ENSP00000354859.3:p.Val421=
ENST00000538967.5:c.1268T= ENSP00000438215.1:p.Val423=
ENST00000542968.5:c.1262T= ENSP00000442172.1:p.Val421=
ENST00000544518.5:c.1259T= ENSP00000441068.1:p.Val420=
NM_000795.3:c.1262T= NP_000786.1:p.Val421=
NM_016574.3:c.1175T= NP_057658.2:p.Val392=
XM_017017296.2:c.1262T= XP_016872785.1:p.Val421=
NM_000795.4:c.1262T= MANE Select NP_000786.1:p.Val421=
NM_016574.4:c.1175T= NP_057658.2:p.Val392=