Canonical Allele Identifier: CA677045003

Gene: NDUFS3

Linked Data

• dbSNP Id: rs1465295575
• gnomAD v3: 11-47582279-A-G
• gnomAD v4: 11-47582279-A-G
• MyVariant Identifiers: chr11:g.47603831A>G (hg19) ; chr11:g.47582279A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582279A>G , CM000673.2:g.47582279A>G	GRCh38
NC_000011.9:g.47603831A>G , CM000673.1:g.47603831A>G	GRCh37
NC_000011.8:g.47560407A>G	NCBI36
NG_011946.1:g.8270A>G
NG_011946.2:g.8270A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.507+66A>G MANE Select	ENSP00000263774.4:n.507+66A>G
ENST00000531351.2:n.1633A>G
ENST00000677462.1:n.2981+66A>G
ENST00000678975.1:n.2764+66A>G
ENST00000263774.8:c.507+66A>G	ENSP00000263774.4:n.507+66A>G
ENST00000524568.1:n.610+66A>G
ENST00000525212.1:n.162+66A>G
ENST00000525378.5:n.445+66A>G
ENST00000527178.1:n.38A>G
ENST00000533507.5:n.1401+66A>G
NM_004551.2:c.507+66A>G	NP_004542.1:n.507+66A>G
NM_004551.3:c.507+66A>G MANE Select	NP_004542.1:n.507+66A>G