Canonical Allele Identifier: CA1969461923
Gene: NDUFS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582056C= , CM000673.2:g.47582056C= GRCh38
NC_000011.9:g.47603608C= , CM000673.1:g.47603608C= GRCh37
NC_000011.8:g.47560184C= NCBI36
NG_011946.1:g.8047C=
NG_011946.2:g.8047C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.382-32C= MANE Select ENSP00000263774.4:n.382-32C=
ENST00000531351.2:n.1410C=
ENST00000677462.1:n.2824C=
ENST00000678975.1:n.2607C=
ENST00000263774.8:c.382-32C= ENSP00000263774.4:n.382-32C=
ENST00000524568.1:n.485-32C=
ENST00000525212.1:n.5C=
ENST00000525378.5:n.288C=
ENST00000533507.5:n.1276-32C=
NM_004551.2:c.382-32C= NP_004542.1:n.382-32C=
NM_004551.3:c.382-32C= MANE Select NP_004542.1:n.382-32C=