Canonical Allele Identifier: CA937672241
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs2097269150
gnomAD v3: 11-47582282-C-G
gnomAD v4: 11-47582282-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582282C>G , CM000673.2:g.47582282C>G GRCh38
NC_000011.9:g.47603834C>G , CM000673.1:g.47603834C>G GRCh37
NC_000011.8:g.47560410C>G NCBI36
NG_011946.1:g.8273C>G
NG_011946.2:g.8273C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508-67C>G MANE Select ENSP00000263774.4:n.508-67C>G
ENST00000531351.2:n.1636C>G
ENST00000677462.1:n.2982-67C>G
ENST00000678975.1:n.2765-67C>G
ENST00000263774.8:c.508-67C>G ENSP00000263774.4:n.508-67C>G
ENST00000524568.1:n.611-67C>G
ENST00000525212.1:n.163-67C>G
ENST00000525378.5:n.446-67C>G
ENST00000527178.1:n.41C>G
ENST00000533507.5:n.1402-67C>G
NM_004551.2:c.508-67C>G NP_004542.1:n.508-67C>G
NM_004551.3:c.508-67C>G MANE Select NP_004542.1:n.508-67C>G
Search 100 bp 5'
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