Canonical Allele Identifier: CA228635538
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs200650558

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439318G>T , CM000673.2:g.113439318G>T GRCh38
NC_000011.9:g.113310040G>T , CM000673.1:g.113310040G>T GRCh37
NC_000011.8:g.112815250G>T NCBI36
NG_008841.1:g.40962C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-31-14636C>A MANE Select ENSP00000354859.3:n.-31-14636C>A
ENST00000346454.7:c.-31-14636C>A ENSP00000278597.5:n.-31-14636C>A
ENST00000362072.7:c.-31-14636C>A ENSP00000354859.3:n.-31-14636C>A
ENST00000540600.5:n.35-14636C>A
ENST00000542616.1:c.-31-14636C>A ENSP00000441474.1:n.-31-14636C>A
ENST00000543292.1:c.-32+8253C>A ENSP00000438419.1:n.-32+8253C>A
NM_000795.3:c.-31-14636C>A NP_000786.1:n.-31-14636C>A
NM_016574.3:c.-31-14636C>A NP_057658.2:n.-31-14636C>A
XM_017017296.2:c.-31-14636C>A XP_016872785.1:n.-31-14636C>A
NM_000795.4:c.-31-14636C>A MANE Select NP_000786.1:n.-31-14636C>A
NM_016574.4:c.-31-14636C>A NP_057658.2:n.-31-14636C>A