Canonical Allele Identifier: CA942371450
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1951063362

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439072T>C , CM000673.2:g.113439072T>C GRCh38
NC_000011.9:g.113309794T>C , CM000673.1:g.113309794T>C GRCh37
NC_000011.8:g.112815004T>C NCBI36
NG_008841.1:g.41208A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-31-14390A>G MANE Select ENSP00000354859.3:n.-31-14390A>G
ENST00000346454.7:c.-31-14390A>G ENSP00000278597.5:n.-31-14390A>G
ENST00000362072.7:c.-31-14390A>G ENSP00000354859.3:n.-31-14390A>G
ENST00000540600.5:n.35-14390A>G
ENST00000542616.1:c.-31-14390A>G ENSP00000441474.1:n.-31-14390A>G
ENST00000543292.1:c.-32+8499A>G ENSP00000438419.1:n.-32+8499A>G
NM_000795.3:c.-31-14390A>G NP_000786.1:n.-31-14390A>G
NM_016574.3:c.-31-14390A>G NP_057658.2:n.-31-14390A>G
XM_017017296.2:c.-31-14390A>G XP_016872785.1:n.-31-14390A>G
NM_000795.4:c.-31-14390A>G MANE Select NP_000786.1:n.-31-14390A>G
NM_016574.4:c.-31-14390A>G NP_057658.2:n.-31-14390A>G