Canonical Allele Identifier: CA2703754884
Gene: DRD3 HGNC NCBI

Linked Data

dbSNP Id: rs2077538006

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.114142804A>C , CM000665.2:g.114142804A>C GRCh38
NC_000003.11:g.113861651A>C , CM000665.1:g.113861651A>C GRCh37
NC_000003.10:g.115344341A>C NCBI36
NG_008842.2:g.61604T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698213.1:c.527-3108T>G ENSP00000513607.1:n.527-3108T>G
ENST00000383673.5:c.527-3108T>G MANE Select ENSP00000373169.2:n.527-3108T>G
ENST00000295881.9:c.527-3108T>G ENSP00000295881.6:n.527-3108T>G
ENST00000383673.4:c.527-3108T>G ENSP00000373169.2:n.527-3108T>G
ENST00000460779.5:c.527-3108T>G ENSP00000419402.1:n.527-3108T>G
ENST00000467632.5:c.527-3108T>G ENSP00000420662.1:n.527-3108T>G
NM_000796.5:c.527-3108T>G NP_000787.2:n.527-3108T>G
NM_001282563.2:c.527-3108T>G NP_001269492.1:n.527-3108T>G
NM_001290809.1:c.527-3108T>G NP_001277738.1:n.527-3108T>G
NM_033663.5:c.527-3108T>G NP_387512.3:n.527-3108T>G
XM_011512510.1:c.527-3108T>G XP_011510812.1:n.527-3108T>G
XM_011512511.1:c.527-3108T>G XP_011510813.1:n.527-3108T>G
XM_011512512.1:c.527-3108T>G XP_011510814.1:n.527-3108T>G
XM_017005829.1:c.527-3108T>G XP_016861318.1:n.527-3108T>G
NM_000796.6:c.527-3108T>G MANE Select NP_000787.2:n.527-3108T>G
NM_033663.6:c.527-3108T>G NP_387512.3:n.527-3108T>G