Canonical Allele Identifier: CA474220615
Gene: NDUFS3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.47604002T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582450T>C , CM000673.2:g.47582450T>C GRCh38
NC_000011.9:g.47604002T>C , CM000673.1:g.47604002T>C GRCh37
NC_000011.8:g.47560578T>C NCBI36
NG_011946.1:g.8441T>C
NG_011946.2:g.8441T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263774.9:c.609T>C MANE Select ENSP00000263774.4:p.Pro203=
ENST00000531351.2:n.1804T>C
ENST00000677462.1:n.3083T>C
ENST00000678975.1:n.2866T>C
ENST00000263774.8:c.609T>C ENSP00000263774.4:p.Pro203=
ENST00000524568.1:n.712T>C
ENST00000525212.1:n.264T>C
ENST00000525378.5:n.547T>C
ENST00000527178.1:n.209T>C
ENST00000533507.5:n.1503T>C
NM_004551.2:c.609T>C NP_004542.1:p.Pro203=
NM_004551.3:c.609T>C MANE Select NP_004542.1:p.Pro203=
Search 100 bp 5'
Search 100 bp 3'