Canonical Allele Identifier: CA397761555
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1567670943
MyVariant Identifiers: chr17:g.6683803C>T (hg19) chr17:g.6780484C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780484C>T , CM000679.2:g.6780484C>T GRCh38
NC_000017.10:g.6683803C>T , CM000679.1:g.6683803C>T GRCh37
NC_000017.9:g.6624527C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.616C>T MANE Select ENSP00000321386.4:p.His206Tyr
ENST00000321535.4:c.616C>T ENSP00000321386.4:p.His206Tyr
NM_153230.2:c.616C>T NP_694962.1:p.His206Tyr
XM_011523697.1:c.616C>T XP_011521999.1:p.His206Tyr
XR_243544.3:n.794C>T
NM_153230.3:c.616C>T MANE Select NP_694962.1:p.His206Tyr
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