Canonical Allele Identifier: CA2001161873

Gene: DRD2

Linked Data

• dbSNP Id: rs1951105592

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442670C>G , CM000673.2:g.113442670C>G	GRCh38
NC_000011.9:g.113313392C>G , CM000673.1:g.113313392C>G	GRCh37
NC_000011.8:g.112818602C>G	NCBI36
NG_008841.1:g.37610G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-17988G>C MANE Select	ENSP00000354859.3:n.-31-17988G>C
ENST00000346454.7:c.-31-17988G>C	ENSP00000278597.5:n.-31-17988G>C
ENST00000362072.7:c.-31-17988G>C	ENSP00000354859.3:n.-31-17988G>C
ENST00000540600.5:n.35-17988G>C
ENST00000542616.1:c.-31-17988G>C	ENSP00000441474.1:n.-31-17988G>C
ENST00000543292.1:c.-32+4901G>C	ENSP00000438419.1:n.-32+4901G>C
NM_000795.3:c.-31-17988G>C	NP_000786.1:n.-31-17988G>C
NM_016574.3:c.-31-17988G>C	NP_057658.2:n.-31-17988G>C
XM_017017296.2:c.-31-17988G>C	XP_016872785.1:n.-31-17988G>C
NM_000795.4:c.-31-17988G>C MANE Select	NP_000786.1:n.-31-17988G>C
NM_016574.4:c.-31-17988G>C	NP_057658.2:n.-31-17988G>C