Canonical Allele Identifier: CA221735652

Gene: NDUFS3

Linked Data

• dbSNP Id: rs2233358
• gnomAD v4: 11-47582275-C-G
• MyVariant Identifiers: chr11:g.47582275C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582275C>G , CM000673.2:g.47582275C>G	GRCh38
NC_000011.9:g.47603827C>G , CM000673.1:g.47603827C>G	GRCh37
NC_000011.8:g.47560403C>G	NCBI36
NG_011946.1:g.8266C>G
NG_011946.2:g.8266C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.507+62C>G MANE Select	ENSP00000263774.4:n.507+62C>G
ENST00000531351.2:n.1629C>G
ENST00000677462.1:n.2981+62C>G
ENST00000678975.1:n.2764+62C>G
ENST00000263774.8:c.507+62C>G	ENSP00000263774.4:n.507+62C>G
ENST00000524568.1:n.610+62C>G
ENST00000525212.1:n.162+62C>G
ENST00000525378.5:n.445+62C>G
ENST00000527178.1:n.34C>G
ENST00000533507.5:n.1401+62C>G
NM_004551.2:c.507+62C>G	NP_004542.1:n.507+62C>G
NM_004551.3:c.507+62C>G MANE Select	NP_004542.1:n.507+62C>G