Canonical Allele Identifier: CA2501469999

Gene: DRD2

Linked Data

• dbSNP Id: rs2119845682
• gnomAD v3: 11-113438990-CT-C
• gnomAD v4: 11-113438990-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113438991del , CM000673.2:g.113438991del	GRCh38
NC_000011.9:g.113309713del , CM000673.1:g.113309713del	GRCh37
NC_000011.8:g.112814923del	NCBI36
NG_008841.1:g.41289del

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-14309del MANE Select	ENSP00000354859.3:n.-31-14309del
ENST00000346454.7:c.-31-14309del	ENSP00000278597.5:n.-31-14309del
ENST00000362072.7:c.-31-14309del	ENSP00000354859.3:n.-31-14309del
ENST00000540600.5:n.35-14309del
ENST00000542616.1:c.-31-14309del	ENSP00000441474.1:n.-31-14309del
ENST00000543292.1:c.-32+8580del	ENSP00000438419.1:n.-32+8580del
NM_000795.3:c.-31-14309del	NP_000786.1:n.-31-14309del
NM_016574.3:c.-31-14309del	NP_057658.2:n.-31-14309del
XM_017017296.2:c.-31-14309del	XP_016872785.1:n.-31-14309del
NM_000795.4:c.-31-14309del MANE Select	NP_000786.1:n.-31-14309del
NM_016574.4:c.-31-14309del	NP_057658.2:n.-31-14309del