Canonical Allele Identifier: CA474432229

Gene: NDUFS3

Linked Data

• MyVariant Identifiers: chr11:g.47603960A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47582408A>T , CM000673.2:g.47582408A>T	GRCh38
NC_000011.9:g.47603960A>T , CM000673.1:g.47603960A>T	GRCh37
NC_000011.8:g.47560536A>T	NCBI36
NG_011946.1:g.8399A>T
NG_011946.2:g.8399A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263774.9:c.567A>T MANE Select	ENSP00000263774.4:p.Thr189=
ENST00000531351.2:n.1762A>T
ENST00000677462.1:n.3041A>T
ENST00000678975.1:n.2824A>T
ENST00000263774.8:c.567A>T	ENSP00000263774.4:p.Thr189=
ENST00000524568.1:n.670A>T
ENST00000525212.1:n.222A>T
ENST00000525378.5:n.505A>T
ENST00000527178.1:n.167A>T
ENST00000533507.5:n.1461A>T
NM_004551.2:c.567A>T	NP_004542.1:p.Thr189=
NM_004551.3:c.567A>T MANE Select	NP_004542.1:p.Thr189=