Canonical Allele Identifier: CA671867322

Gene: DRD2

Linked Data

• dbSNP Id: rs1217845865
• gnomAD v3: 11-113414807-AG-A
• gnomAD v4: 11-113414807-AG-A
• MyVariant Identifiers: chr11:g.113285530del (hg19) ; chr11:g.113414808del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414809del , CM000673.2:g.113414809del	GRCh38
NC_000011.9:g.113285531del , CM000673.1:g.113285531del	GRCh37
NC_000011.8:g.112790741del	NCBI36
NG_008841.1:g.65472del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-347del MANE Select	ENSP00000354859.3:n.724-347del
ENST00000346454.7:c.723+613del	ENSP00000278597.5:n.723+613del
ENST00000362072.7:c.724-347del	ENSP00000354859.3:n.724-347del
ENST00000535984.1:n.443-347del
ENST00000538967.5:c.724-347del	ENSP00000438215.1:n.724-347del
ENST00000540600.5:n.789-347del
ENST00000542968.5:c.724-347del	ENSP00000442172.1:n.724-347del
ENST00000544518.5:c.721-347del	ENSP00000441068.1:n.721-347del
NM_000795.3:c.724-347del	NP_000786.1:n.724-347del
NM_016574.3:c.723+613del	NP_057658.2:n.723+613del
XM_017017296.2:c.724-347del	XP_016872785.1:n.724-347del
NM_000795.4:c.724-347del MANE Select	NP_000786.1:n.724-347del
NM_016574.4:c.723+613del	NP_057658.2:n.723+613del