Canonical Allele Identifier: CA6281485
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113424520G>A , CM000673.2:g.113424520G>A GRCh38
NC_000011.9:g.113295242G>A , CM000673.1:g.113295242G>A GRCh37
NC_000011.8:g.112800452G>A NCBI36
NG_008841.1:g.55760C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.132C>T MANE Select ENSP00000354859.3:p.Leu44=
ENST00000346454.7:c.132C>T ENSP00000278597.5:p.Leu44=
ENST00000362072.7:c.132C>T ENSP00000354859.3:p.Leu44=
ENST00000538967.5:c.132C>T ENSP00000438215.1:p.Leu44=
ENST00000540600.5:n.197C>T
ENST00000542968.5:c.132C>T ENSP00000442172.1:p.Leu44=
ENST00000543292.1:c.132C>T ENSP00000438419.1:p.Leu44=
ENST00000544518.5:c.132C>T ENSP00000441068.1:p.Leu44=
NM_000795.3:c.132C>T NP_000786.1:p.Leu44=
NM_016574.3:c.132C>T NP_057658.2:p.Leu44=
XM_017017296.2:c.132C>T XP_016872785.1:p.Leu44=
NM_000795.4:c.132C>T MANE Select NP_000786.1:p.Leu44=
NM_016574.4:c.132C>T NP_057658.2:p.Leu44=