Canonical Allele Identifier: CA81692529

Gene: DRD3

Linked Data

• dbSNP Id: rs2630349
• gnomAD v2: 3-113873372-A-G
• gnomAD v3: 3-114154525-A-G
• gnomAD v4: 3-114154525-A-G
• MyVariant Identifiers: chr3:g.113873372A>G (hg19) ; chr3:g.114154525A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114154525A>G , CM000665.2:g.114154525A>G	GRCh38
NC_000003.11:g.113873372A>G , CM000665.1:g.113873372A>G	GRCh37
NC_000003.10:g.115356062A>G	NCBI36
NG_008842.2:g.49883T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698213.1:c.383+5230T>C	ENSP00000513607.1:n.383+5230T>C
ENST00000383673.5:c.383+5230T>C MANE Select	ENSP00000373169.2:n.383+5230T>C
ENST00000295881.9:c.383+5230T>C	ENSP00000295881.6:n.383+5230T>C
ENST00000383673.4:c.383+5230T>C	ENSP00000373169.2:n.383+5230T>C
ENST00000460779.5:c.383+5230T>C	ENSP00000419402.1:n.383+5230T>C
ENST00000467632.5:c.383+5230T>C	ENSP00000420662.1:n.383+5230T>C
NM_000796.5:c.383+5230T>C	NP_000787.2:n.383+5230T>C
NM_001282563.2:c.383+5230T>C	NP_001269492.1:n.383+5230T>C
NM_001290809.1:c.383+5230T>C	NP_001277738.1:n.383+5230T>C
NM_033663.5:c.383+5230T>C	NP_387512.3:n.383+5230T>C
XM_011512510.1:c.383+5230T>C	XP_011510812.1:n.383+5230T>C
XM_011512511.1:c.383+5230T>C	XP_011510813.1:n.383+5230T>C
XM_011512512.1:c.383+5230T>C	XP_011510814.1:n.383+5230T>C
XM_017005829.1:c.383+5230T>C	XP_016861318.1:n.383+5230T>C
NM_000796.6:c.383+5230T>C MANE Select	NP_000787.2:n.383+5230T>C
NM_033663.6:c.383+5230T>C	NP_387512.3:n.383+5230T>C