Canonical Allele Identifier: CA2580582572
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414814C>G , CM000673.2:g.113414814C>G GRCh38
NC_000011.9:g.113285536C>G , CM000673.1:g.113285536C>G GRCh37
NC_000011.8:g.112790746C>G NCBI36
NG_008841.1:g.65466G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.724-353G>C MANE Select ENSP00000354859.3:n.724-353G>C
ENST00000346454.7:c.723+607G>C ENSP00000278597.5:n.723+607G>C
ENST00000362072.7:c.724-353G>C ENSP00000354859.3:n.724-353G>C
ENST00000535984.1:n.443-353G>C
ENST00000538967.5:c.724-353G>C ENSP00000438215.1:n.724-353G>C
ENST00000540600.5:n.789-353G>C
ENST00000542968.5:c.724-353G>C ENSP00000442172.1:n.724-353G>C
ENST00000544518.5:c.721-353G>C ENSP00000441068.1:n.721-353G>C
NM_000795.3:c.724-353G>C NP_000786.1:n.724-353G>C
NM_016574.3:c.723+607G>C NP_057658.2:n.723+607G>C
XM_017017296.2:c.724-353G>C XP_016872785.1:n.724-353G>C
NM_000795.4:c.724-353G>C MANE Select NP_000786.1:n.724-353G>C
NM_016574.4:c.723+607G>C NP_057658.2:n.723+607G>C