Canonical Allele Identifier: CA942371198

Gene: DRD2

Linked Data

• dbSNP Id: rs1951105329
• gnomAD v3: 11-113442641-TG-T
• gnomAD v4: 11-113442641-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442644del , CM000673.2:g.113442644del	GRCh38
NC_000011.9:g.113313366del , CM000673.1:g.113313366del	GRCh37
NC_000011.8:g.112818576del	NCBI36
NG_008841.1:g.37638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-17960del MANE Select	ENSP00000354859.3:n.-31-17960del
ENST00000346454.7:c.-31-17960del	ENSP00000278597.5:n.-31-17960del
ENST00000362072.7:c.-31-17960del	ENSP00000354859.3:n.-31-17960del
ENST00000540600.5:n.35-17960del
ENST00000542616.1:c.-31-17960del	ENSP00000441474.1:n.-31-17960del
ENST00000543292.1:c.-32+4929del	ENSP00000438419.1:n.-32+4929del
NM_000795.3:c.-31-17960del	NP_000786.1:n.-31-17960del
NM_016574.3:c.-31-17960del	NP_057658.2:n.-31-17960del
XM_017017296.2:c.-31-17960del	XP_016872785.1:n.-31-17960del
NM_000795.4:c.-31-17960del MANE Select	NP_000786.1:n.-31-17960del
NM_016574.4:c.-31-17960del	NP_057658.2:n.-31-17960del