Canonical Allele Identifier: CA380361531
Gene: NDUFS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582349A>G , CM000673.2:g.47582349A>G GRCh38
NC_000011.9:g.47603901A>G , CM000673.1:g.47603901A>G GRCh37
NC_000011.8:g.47560477A>G NCBI36
NG_011946.1:g.8340A>G
NG_011946.2:g.8340A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508A>G MANE Select ENSP00000263774.4:p.Ile170Val
ENST00000531351.2:n.1703A>G
ENST00000677462.1:n.2982A>G
ENST00000678975.1:n.2765A>G
ENST00000263774.8:c.508A>G ENSP00000263774.4:p.Ile170Val
ENST00000524568.1:n.611A>G
ENST00000525212.1:n.163A>G
ENST00000525378.5:n.446A>G
ENST00000527178.1:n.108A>G
ENST00000533507.5:n.1402A>G
NM_004551.2:c.508A>G NP_004542.1:p.Ile170Val
NM_004551.3:c.508A>G MANE Select NP_004542.1:p.Ile170Val