Canonical Allele Identifier: CA937672245
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs2097269152
gnomAD v3: 11-47582284-G-A
gnomAD v4: 11-47582284-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582284G>A , CM000673.2:g.47582284G>A GRCh38
NC_000011.9:g.47603836G>A , CM000673.1:g.47603836G>A GRCh37
NC_000011.8:g.47560412G>A NCBI36
NG_011946.1:g.8275G>A
NG_011946.2:g.8275G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508-65G>A MANE Select ENSP00000263774.4:n.508-65G>A
ENST00000531351.2:n.1638G>A
ENST00000677462.1:n.2982-65G>A
ENST00000678975.1:n.2765-65G>A
ENST00000263774.8:c.508-65G>A ENSP00000263774.4:n.508-65G>A
ENST00000524568.1:n.611-65G>A
ENST00000525212.1:n.163-65G>A
ENST00000525378.5:n.446-65G>A
ENST00000527178.1:n.43G>A
ENST00000533507.5:n.1402-65G>A
NM_004551.2:c.508-65G>A NP_004542.1:n.508-65G>A
NM_004551.3:c.508-65G>A MANE Select NP_004542.1:n.508-65G>A
Search 100 bp 5'
Search 100 bp 3'