Canonical Allele Identifier: CA2613426595
Gene: NDUFS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582265G>C , CM000673.2:g.47582265G>C GRCh38
NC_000011.9:g.47603817G>C , CM000673.1:g.47603817G>C GRCh37
NC_000011.8:g.47560393G>C NCBI36
NG_011946.1:g.8256G>C
NG_011946.2:g.8256G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.507+52G>C MANE Select ENSP00000263774.4:n.507+52G>C
ENST00000531351.2:n.1619G>C
ENST00000677462.1:n.2981+52G>C
ENST00000678975.1:n.2764+52G>C
ENST00000263774.8:c.507+52G>C ENSP00000263774.4:n.507+52G>C
ENST00000524568.1:n.610+52G>C
ENST00000525212.1:n.162+52G>C
ENST00000525378.5:n.445+52G>C
ENST00000527178.1:n.24G>C
ENST00000533507.5:n.1401+52G>C
NM_004551.2:c.507+52G>C NP_004542.1:n.507+52G>C
NM_004551.3:c.507+52G>C MANE Select NP_004542.1:n.507+52G>C