Canonical Allele Identifier: CA2613426648
Gene: NDUFS3 HGNC NCBI

Linked Data

gnomAD v4: 11-47582344-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582344C>A , CM000673.2:g.47582344C>A GRCh38
NC_000011.9:g.47603896C>A , CM000673.1:g.47603896C>A GRCh37
NC_000011.8:g.47560472C>A NCBI36
NG_011946.1:g.8335C>A
NG_011946.2:g.8335C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508-5C>A MANE Select ENSP00000263774.4:n.508-5C>A
ENST00000531351.2:n.1698C>A
ENST00000677462.1:n.2982-5C>A
ENST00000678975.1:n.2765-5C>A
ENST00000263774.8:c.508-5C>A ENSP00000263774.4:n.508-5C>A
ENST00000524568.1:n.611-5C>A
ENST00000525212.1:n.163-5C>A
ENST00000525378.5:n.446-5C>A
ENST00000527178.1:n.103C>A
ENST00000533507.5:n.1402-5C>A
NM_004551.2:c.508-5C>A NP_004542.1:n.508-5C>A
NM_004551.3:c.508-5C>A MANE Select NP_004542.1:n.508-5C>A
Search 100 bp 5'
Search 100 bp 3'