Canonical Allele Identifier: CA2001159447

Gene: DRD2

Linked Data

• dbSNP Id: rs1951063176

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439045_113439052del , CM000673.2:g.113439045_113439052del	GRCh38
NC_000011.9:g.113309767_113309774del , CM000673.1:g.113309767_113309774del	GRCh37
NC_000011.8:g.112814977_112814984del	NCBI36
NG_008841.1:g.41230_41237del

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-14368_-31-14361del MANE Select	ENSP00000354859.3:n.-31-14368_-31-14361de...
ENST00000346454.7:c.-31-14368_-31-14361del	ENSP00000278597.5:n.-31-14368_-31-14361de...
ENST00000362072.7:c.-31-14368_-31-14361del	ENSP00000354859.3:n.-31-14368_-31-14361de...
ENST00000540600.5:n.35-14368_35-14361del
ENST00000542616.1:c.-31-14368_-31-14361del	ENSP00000441474.1:n.-31-14368_-31-14361de...
ENST00000543292.1:c.-32+8521_-32+8528del	ENSP00000438419.1:n.-32+8521_-32+8528del
NM_000795.3:c.-31-14368_-31-14361del	NP_000786.1:n.-31-14368_-31-14361del
NM_016574.3:c.-31-14368_-31-14361del	NP_057658.2:n.-31-14368_-31-14361del
XM_017017296.2:c.-31-14368_-31-14361del	XP_016872785.1:n.-31-14368_-31-14361del
NM_000795.4:c.-31-14368_-31-14361del MANE Select	NP_000786.1:n.-31-14368_-31-14361del
NM_016574.4:c.-31-14368_-31-14361del	NP_057658.2:n.-31-14368_-31-14361del