Canonical Allele Identifier: CA228625588
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs202098964

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412624G>A , CM000673.2:g.113412624G>A GRCh38
NC_000011.9:g.113283346G>A , CM000673.1:g.113283346G>A GRCh37
NC_000011.8:g.112788556G>A NCBI36
NG_008841.1:g.67656C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1070C>T MANE Select ENSP00000354859.3:p.Thr357Ile
ENST00000346454.7:c.983C>T ENSP00000278597.5:p.Thr328Ile
ENST00000362072.7:c.1070C>T ENSP00000354859.3:p.Thr357Ile
ENST00000538967.5:c.1076C>T ENSP00000438215.1:p.Thr359Ile
ENST00000542968.5:c.1070C>T ENSP00000442172.1:p.Thr357Ile
ENST00000544518.5:c.1067C>T ENSP00000441068.1:p.Thr356Ile
NM_000795.3:c.1070C>T NP_000786.1:p.Thr357Ile
NM_016574.3:c.983C>T NP_057658.2:p.Thr328Ile
XM_017017296.2:c.1070C>T XP_016872785.1:p.Thr357Ile
NM_000795.4:c.1070C>T MANE Select NP_000786.1:p.Thr357Ile
NM_016574.4:c.983C>T NP_057658.2:p.Thr328Ile