Canonical Allele Identifier: CA2613426652
Gene: NDUFS3 HGNC NCBI

Linked Data

gnomAD v4: 11-47582346-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582346T>C , CM000673.2:g.47582346T>C GRCh38
NC_000011.9:g.47603898T>C , CM000673.1:g.47603898T>C GRCh37
NC_000011.8:g.47560474T>C NCBI36
NG_011946.1:g.8337T>C
NG_011946.2:g.8337T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508-3T>C MANE Select ENSP00000263774.4:n.508-3T>C
ENST00000531351.2:n.1700T>C
ENST00000677462.1:n.2982-3T>C
ENST00000678975.1:n.2765-3T>C
ENST00000263774.8:c.508-3T>C ENSP00000263774.4:n.508-3T>C
ENST00000524568.1:n.611-3T>C
ENST00000525212.1:n.163-3T>C
ENST00000525378.5:n.446-3T>C
ENST00000527178.1:n.105T>C
ENST00000533507.5:n.1402-3T>C
NM_004551.2:c.508-3T>C NP_004542.1:n.508-3T>C
NM_004551.3:c.508-3T>C MANE Select NP_004542.1:n.508-3T>C
Search 100 bp 5'
Search 100 bp 3'