Canonical Allele Identifier: CA2613426589
Gene: NDUFS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582253G>A , CM000673.2:g.47582253G>A GRCh38
NC_000011.9:g.47603805G>A , CM000673.1:g.47603805G>A GRCh37
NC_000011.8:g.47560381G>A NCBI36
NG_011946.1:g.8244G>A
NG_011946.2:g.8244G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.507+40G>A MANE Select ENSP00000263774.4:n.507+40G>A
ENST00000531351.2:n.1607G>A
ENST00000677462.1:n.2981+40G>A
ENST00000678975.1:n.2764+40G>A
ENST00000263774.8:c.507+40G>A ENSP00000263774.4:n.507+40G>A
ENST00000524568.1:n.610+40G>A
ENST00000525212.1:n.162+40G>A
ENST00000525378.5:n.445+40G>A
ENST00000527178.1:n.12G>A
ENST00000533507.5:n.1401+40G>A
NM_004551.2:c.507+40G>A NP_004542.1:n.507+40G>A
NM_004551.3:c.507+40G>A MANE Select NP_004542.1:n.507+40G>A