Canonical Allele Identifier: CA5978009
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs770264683
ExAC: 11:47603797 G / A
gnomAD v2: 11-47603797-G-A
gnomAD v3: 11-47582245-G-A
gnomAD v4: 11-47582245-G-A
MyVariant Identifiers: chr11:g.47603797G>A (hg19) chr11:g.47582245G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582245G>A , CM000673.2:g.47582245G>A GRCh38
NC_000011.9:g.47603797G>A , CM000673.1:g.47603797G>A GRCh37
NC_000011.8:g.47560373G>A NCBI36
NG_011946.1:g.8236G>A
NG_011946.2:g.8236G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.507+32G>A MANE Select ENSP00000263774.4:n.507+32G>A
ENST00000531351.2:n.1599G>A
ENST00000677462.1:n.2981+32G>A
ENST00000678975.1:n.2764+32G>A
ENST00000263774.8:c.507+32G>A ENSP00000263774.4:n.507+32G>A
ENST00000524568.1:n.610+32G>A
ENST00000525212.1:n.162+32G>A
ENST00000525378.5:n.445+32G>A
ENST00000527178.1:n.4G>A
ENST00000533507.5:n.1401+32G>A
NM_004551.2:c.507+32G>A NP_004542.1:n.507+32G>A
NM_004551.3:c.507+32G>A MANE Select NP_004542.1:n.507+32G>A
Search 100 bp 5'
Search 100 bp 3'