Canonical Allele Identifier: CA1969462116
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582279A= , CM000673.2:g.47582279A= GRCh38
NC_000011.9:g.47603831A= , CM000673.1:g.47603831A= GRCh37
NC_000011.8:g.47560407A= NCBI36
NG_011946.1:g.8270A=
NG_011946.2:g.8270A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.507+66A= MANE Select ENSP00000263774.4:n.507+66A=
ENST00000531351.2:n.1633A=
ENST00000677462.1:n.2981+66A=
ENST00000678975.1:n.2764+66A=
ENST00000263774.8:c.507+66A= ENSP00000263774.4:n.507+66A=
ENST00000524568.1:n.610+66A=
ENST00000525212.1:n.162+66A=
ENST00000525378.5:n.445+66A=
ENST00000527178.1:n.38A=
ENST00000533507.5:n.1401+66A=
NM_004551.2:c.507+66A= NP_004542.1:n.507+66A=
NM_004551.3:c.507+66A= MANE Select NP_004542.1:n.507+66A=