Canonical Allele Identifier: CA677045004
Gene: NDUFS3 HGNC NCBI

Linked Data

dbSNP Id: rs1395281985
MyVariant Identifiers: chr11:g.47603835A>G (hg19) chr11:g.47582283A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47582283A>G , CM000673.2:g.47582283A>G GRCh38
NC_000011.9:g.47603835A>G , CM000673.1:g.47603835A>G GRCh37
NC_000011.8:g.47560411A>G NCBI36
NG_011946.1:g.8274A>G
NG_011946.2:g.8274A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263774.9:c.508-66A>G MANE Select ENSP00000263774.4:n.508-66A>G
ENST00000531351.2:n.1637A>G
ENST00000677462.1:n.2982-66A>G
ENST00000678975.1:n.2765-66A>G
ENST00000263774.8:c.508-66A>G ENSP00000263774.4:n.508-66A>G
ENST00000524568.1:n.611-66A>G
ENST00000525212.1:n.163-66A>G
ENST00000525378.5:n.446-66A>G
ENST00000527178.1:n.42A>G
ENST00000533507.5:n.1402-66A>G
NM_004551.2:c.508-66A>G NP_004542.1:n.508-66A>G
NM_004551.3:c.508-66A>G MANE Select NP_004542.1:n.508-66A>G
Search 100 bp 5'
Search 100 bp 3'