Canonical Allele Identifier: CA11416597

Gene: DRD3

Linked Data

• dbSNP Id: rs4646996
• gnomAD v2: 3-113849565-C-T
• gnomAD v3: 3-114130718-C-T
• gnomAD v4: 3-114130718-C-T
• MyVariant Identifiers: chr3:g.113849565C>T (hg19) ; chr3:g.114130718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114130718C>T , CM000665.2:g.114130718C>T	GRCh38
NC_000003.11:g.113849565C>T , CM000665.1:g.113849565C>T	GRCh37
NC_000003.10:g.115332255C>T	NCBI36
NG_008842.2:g.73690G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698213.1:c.*310+400G>A	ENSP00000513607.1:n.*310+400G>A
ENST00000383673.5:c.1006+400G>A MANE Select	ENSP00000373169.2:n.1006+400G>A
ENST00000295881.9:c.907+400G>A	ENSP00000295881.6:n.907+400G>A
ENST00000383673.4:c.1006+400G>A	ENSP00000373169.2:n.1006+400G>A
ENST00000460779.5:c.1006+400G>A	ENSP00000419402.1:n.1006+400G>A
ENST00000467632.5:c.1006+400G>A	ENSP00000420662.1:n.1006+400G>A
NM_000796.5:c.1006+400G>A	NP_000787.2:n.1006+400G>A
NM_001282563.2:c.1006+400G>A	NP_001269492.1:n.1006+400G>A
NM_001290809.1:c.1006+400G>A	NP_001277738.1:n.1006+400G>A
NM_033663.5:c.907+400G>A	NP_387512.3:n.907+400G>A
XM_011512510.1:c.1006+400G>A	XP_011510812.1:n.1006+400G>A
XM_011512511.1:c.1006+400G>A	XP_011510813.1:n.1006+400G>A
XM_011512512.1:c.1006+400G>A	XP_011510814.1:n.1006+400G>A
XM_017005829.1:c.1006+400G>A	XP_016861318.1:n.1006+400G>A
NM_000796.6:c.1006+400G>A MANE Select	NP_000787.2:n.1006+400G>A
NM_033663.6:c.907+400G>A	NP_387512.3:n.907+400G>A