Canonical Allele Identifier: CA2613426591
Gene: NDUFS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582258A>G , CM000673.2:g.47582258A>G GRCh38
NC_000011.9:g.47603810A>G , CM000673.1:g.47603810A>G GRCh37
NC_000011.8:g.47560386A>G NCBI36
NG_011946.1:g.8249A>G
NG_011946.2:g.8249A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.507+45A>G MANE Select ENSP00000263774.4:n.507+45A>G
ENST00000531351.2:n.1612A>G
ENST00000677462.1:n.2981+45A>G
ENST00000678975.1:n.2764+45A>G
ENST00000263774.8:c.507+45A>G ENSP00000263774.4:n.507+45A>G
ENST00000524568.1:n.610+45A>G
ENST00000525212.1:n.162+45A>G
ENST00000525378.5:n.445+45A>G
ENST00000527178.1:n.17A>G
ENST00000533507.5:n.1401+45A>G
NM_004551.2:c.507+45A>G NP_004542.1:n.507+45A>G
NM_004551.3:c.507+45A>G MANE Select NP_004542.1:n.507+45A>G