Canonical Allele Identifier: CA1969462253
Gene: NDUFS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582600C= , CM000673.2:g.47582600C= GRCh38
NC_000011.9:g.47604152C= , CM000673.1:g.47604152C= GRCh37
NC_000011.8:g.47560728C= NCBI36
NG_011946.1:g.8591C=
NG_011946.2:g.8591C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.627+132C= MANE Select ENSP00000263774.4:n.627+132C=
ENST00000531351.2:n.1822+132C=
ENST00000677462.1:n.3101+132C=
ENST00000678975.1:n.2884+132C=
ENST00000263774.8:c.627+132C= ENSP00000263774.4:n.627+132C=
ENST00000525212.1:n.282+132C=
ENST00000525378.5:n.565+132C=
ENST00000527178.1:n.227+132C=
ENST00000533507.5:n.1521+132C=
NM_004551.2:c.627+132C= NP_004542.1:n.627+132C=
NM_004551.3:c.627+132C= MANE Select NP_004542.1:n.627+132C=
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