Canonical Allele Identifier: CA2550540

Gene: DRD3

Linked Data

• ClinVar Variation Id: 342598
• ClinVar RCV Id: RCV000370469
• dbSNP Id: rs2251177
• ExAC: 3:113858350 C / T
• gnomAD v2: 3-113858350-C-T
• gnomAD v3: 3-114139503-C-T
• gnomAD v4: 3-114139503-C-T
• MyVariant Identifiers: chr3:g.113858350C>T (hg19) ; chr3:g.114139503C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114139503C>T , CM000665.2:g.114139503C>T	GRCh38
NC_000003.11:g.113858350C>T , CM000665.1:g.113858350C>T	GRCh37
NC_000003.10:g.115341040C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000698213.1:c.720G>A	ENSP00000513607.1:p.Gln240=
ENST00000383673.5:c.720G>A MANE Select	ENSP00000373169.2:p.Gln240=
ENST00000295881.9:c.720G>A	ENSP00000295881.6:p.Gln240=
ENST00000383673.4:c.720G>A	ENSP00000373169.2:p.Gln240=
ENST00000460779.5:c.720G>A	ENSP00000419402.1:p.Gln240=
ENST00000467632.5:c.720G>A	ENSP00000420662.1:p.Gln240=
XM_011512510.1:c.720G>A	XP_011510812.1:p.Gln240=
XM_011512511.1:c.720G>A	XP_011510813.1:p.Gln240=
XM_011512512.1:c.720G>A	XP_011510814.1:p.Gln240=
XM_017005829.1:c.720G>A	XP_016861318.1:p.Gln240=
NM_000796.6:c.720G>A MANE Select	NP_000787.2:p.Gln240=
NM_033663.6:c.720G>A	NP_387512.3:p.Gln240=