Canonical Allele Identifier: CA380362037

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47604001C>G (hg19) ; chr11:g.47582449C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582449C>G , CM000673.2:g.47582449C>G	GRCh38
NC_000011.9:g.47604001C>G , CM000673.1:g.47604001C>G	GRCh37
NC_000011.8:g.47560577C>G	NCBI36
NG_011946.1:g.8440C>G
NG_011946.2:g.8440C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.608C>G MANE Select	ENSP00000263774.4:p.Pro203Arg
ENST00000531351.2:n.1803C>G
ENST00000677462.1:n.3082C>G
ENST00000678975.1:n.2865C>G
ENST00000263774.8:c.608C>G	ENSP00000263774.4:p.Pro203Arg
ENST00000524568.1:n.711C>G
ENST00000525212.1:n.263C>G
ENST00000525378.5:n.546C>G
ENST00000527178.1:n.208C>G
ENST00000533507.5:n.1502C>G
NM_004551.2:c.608C>G	NP_004542.1:p.Pro203Arg
NM_004551.3:c.608C>G MANE Select	NP_004542.1:p.Pro203Arg