Canonical Allele Identifier: CA1969462254
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs2097269283
gnomAD v4: 11-47582600-C-A
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Genomic Alleles

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

Transcript Alleles

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