Canonical Allele Identifier: CA2613426600
Gene: NDUFS3 HGNC NCBI

Linked Data

gnomAD v4: 11-47582277-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582277G>C , CM000673.2:g.47582277G>C GRCh38
NC_000011.9:g.47603829G>C , CM000673.1:g.47603829G>C GRCh37
NC_000011.8:g.47560405G>C NCBI36
NG_011946.1:g.8268G>C
NG_011946.2:g.8268G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.507+64G>C MANE Select ENSP00000263774.4:n.507+64G>C
ENST00000531351.2:n.1631G>C
ENST00000677462.1:n.2981+64G>C
ENST00000678975.1:n.2764+64G>C
ENST00000263774.8:c.507+64G>C ENSP00000263774.4:n.507+64G>C
ENST00000524568.1:n.610+64G>C
ENST00000525212.1:n.162+64G>C
ENST00000525378.5:n.445+64G>C
ENST00000527178.1:n.36G>C
ENST00000533507.5:n.1401+64G>C
NM_004551.2:c.507+64G>C NP_004542.1:n.507+64G>C
NM_004551.3:c.507+64G>C MANE Select NP_004542.1:n.507+64G>C
Search 100 bp 5'
Search 100 bp 3'