Canonical Allele Identifier: CA474220624

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47604011C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582459C>G , CM000673.2:g.47582459C>G	GRCh38
NC_000011.9:g.47604011C>G , CM000673.1:g.47604011C>G	GRCh37
NC_000011.8:g.47560587C>G	NCBI36
NG_011946.1:g.8450C>G
NG_011946.2:g.8450C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.618C>G MANE Select	ENSP00000263774.4:p.Gly206=
ENST00000531351.2:n.1813C>G
ENST00000677462.1:n.3092C>G
ENST00000678975.1:n.2875C>G
ENST00000263774.8:c.618C>G	ENSP00000263774.4:p.Gly206=
ENST00000524568.1:n.721C>G
ENST00000525212.1:n.273C>G
ENST00000525378.5:n.556C>G
ENST00000527178.1:n.218C>G
ENST00000533507.5:n.1512C>G
NM_004551.2:c.618C>G	NP_004542.1:p.Gly206=
NM_004551.3:c.618C>G MANE Select	NP_004542.1:p.Gly206=