Canonical Allele Identifier: CA897339444

Gene: DRD3

Linked Data

• dbSNP Id: rs1335870195
• MyVariant Identifiers: chr3:g.113849489C>G (hg19) ; chr3:g.114130642C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114130642C>G , CM000665.2:g.114130642C>G	GRCh38
NC_000003.11:g.113849489C>G , CM000665.1:g.113849489C>G	GRCh37
NC_000003.10:g.115332179C>G	NCBI36
NG_008842.2:g.73766G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698213.1:c.*310+476G>C	ENSP00000513607.1:n.*310+476G>C
ENST00000383673.5:c.1006+476G>C MANE Select	ENSP00000373169.2:n.1006+476G>C
ENST00000295881.9:c.907+476G>C	ENSP00000295881.6:n.907+476G>C
ENST00000383673.4:c.1006+476G>C	ENSP00000373169.2:n.1006+476G>C
ENST00000460779.5:c.1006+476G>C	ENSP00000419402.1:n.1006+476G>C
ENST00000467632.5:c.1006+476G>C	ENSP00000420662.1:n.1006+476G>C
NM_000796.5:c.1006+476G>C	NP_000787.2:n.1006+476G>C
NM_001282563.2:c.1006+476G>C	NP_001269492.1:n.1006+476G>C
NM_001290809.1:c.1006+476G>C	NP_001277738.1:n.1006+476G>C
NM_033663.5:c.907+476G>C	NP_387512.3:n.907+476G>C
XM_011512510.1:c.1006+476G>C	XP_011510812.1:n.1006+476G>C
XM_011512511.1:c.1006+476G>C	XP_011510813.1:n.1006+476G>C
XM_011512512.1:c.1006+476G>C	XP_011510814.1:n.1006+476G>C
XM_017005829.1:c.1006+476G>C	XP_016861318.1:n.1006+476G>C
NM_000796.6:c.1006+476G>C MANE Select	NP_000787.2:n.1006+476G>C
NM_033663.6:c.907+476G>C	NP_387512.3:n.907+476G>C