Canonical Allele Identifier: CA474220616

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47604002T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582450T>G , CM000673.2:g.47582450T>G	GRCh38
NC_000011.9:g.47604002T>G , CM000673.1:g.47604002T>G	GRCh37
NC_000011.8:g.47560578T>G	NCBI36
NG_011946.1:g.8441T>G
NG_011946.2:g.8441T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263774.9:c.609T>G MANE Select	ENSP00000263774.4:p.Pro203=
ENST00000531351.2:n.1804T>G
ENST00000677462.1:n.3083T>G
ENST00000678975.1:n.2866T>G
ENST00000263774.8:c.609T>G	ENSP00000263774.4:p.Pro203=
ENST00000524568.1:n.712T>G
ENST00000525212.1:n.264T>G
ENST00000525378.5:n.547T>G
ENST00000527178.1:n.209T>G
ENST00000533507.5:n.1503T>G
NM_004551.2:c.609T>G	NP_004542.1:p.Pro203=
NM_004551.3:c.609T>G MANE Select	NP_004542.1:p.Pro203=