Canonical Allele Identifier: CA382650243
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1199434420

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412751G>T , CM000673.2:g.113412751G>T GRCh38
NC_000011.9:g.113283473G>T , CM000673.1:g.113283473G>T GRCh37
NC_000011.8:g.112788683G>T NCBI36
NG_008841.1:g.67529C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.943C>A MANE Select ENSP00000354859.3:p.Leu315Ile
ENST00000346454.7:c.856C>A ENSP00000278597.5:p.Leu286Ile
ENST00000362072.7:c.943C>A ENSP00000354859.3:p.Leu315Ile
ENST00000538967.5:c.949C>A ENSP00000438215.1:p.Leu317Ile
ENST00000542968.5:c.943C>A ENSP00000442172.1:p.Leu315Ile
ENST00000544518.5:c.940C>A ENSP00000441068.1:p.Leu314Ile
NM_000795.3:c.943C>A NP_000786.1:p.Leu315Ile
NM_016574.3:c.856C>A NP_057658.2:p.Leu286Ile
XM_017017296.2:c.943C>A XP_016872785.1:p.Leu315Ile
NM_000795.4:c.943C>A MANE Select NP_000786.1:p.Leu315Ile
NM_016574.4:c.856C>A NP_057658.2:p.Leu286Ile