Canonical Allele Identifier: CA2001168114
Community Standard Title: NM_000795.4(DRD2):c.811-83G=
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412966C= , CM000673.2:g.113412966C= GRCh38
NC_000011.9:g.113283688C= , CM000673.1:g.113283688C= GRCh37
NC_000011.8:g.112788898C= NCBI36
NG_008841.1:g.67314G=

Transcript Alleles

HGVS Amino-acid Change
NM_000795.4:c.811-83G= MANE Select NP_000786.1:n.811-83G=
ENST00000362072.8:c.811-83G= MANE Select ENSP00000354859.3:n.811-83G=
NM_000795.3:c.811-83G= NP_000786.1:n.811-83G=
NM_016574.3:c.724-83G= NP_057658.2:n.724-83G=
NM_016574.4:c.724-83G= NP_057658.2:n.724-83G=
ENST00000346454.7:c.724-83G= ENSP00000278597.5:n.724-83G=
ENST00000362072.7:c.811-83G= ENSP00000354859.3:n.811-83G=
ENST00000538967.5:c.817-83G= ENSP00000438215.1:n.817-83G=
ENST00000542968.5:c.811-83G= ENSP00000442172.1:n.811-83G=
ENST00000544518.5:c.808-83G= ENSP00000441068.1:n.808-83G=
XM_017017296.2:c.811-83G= XP_016872785.1:n.811-83G=