Canonical Allele Identifier: CA2613426592

Gene: NDUFS3

Linked Data

• gnomAD v4: 11-47582259-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582259G>C , CM000673.2:g.47582259G>C	GRCh38
NC_000011.9:g.47603811G>C , CM000673.1:g.47603811G>C	GRCh37
NC_000011.8:g.47560387G>C	NCBI36
NG_011946.1:g.8250G>C
NG_011946.2:g.8250G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.507+46G>C MANE Select	ENSP00000263774.4:n.507+46G>C
ENST00000531351.2:n.1613G>C
ENST00000677462.1:n.2981+46G>C
ENST00000678975.1:n.2764+46G>C
ENST00000263774.8:c.507+46G>C	ENSP00000263774.4:n.507+46G>C
ENST00000524568.1:n.610+46G>C
ENST00000525212.1:n.162+46G>C
ENST00000525378.5:n.445+46G>C
ENST00000527178.1:n.18G>C
ENST00000533507.5:n.1401+46G>C
NM_004551.2:c.507+46G>C	NP_004542.1:n.507+46G>C
NM_004551.3:c.507+46G>C MANE Select	NP_004542.1:n.507+46G>C