Canonical Allele Identifier: CA397762468
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684050T>A (hg19) chr17:g.6780731T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780731T>A , CM000679.2:g.6780731T>A GRCh38
NC_000017.10:g.6684050T>A , CM000679.1:g.6684050T>A GRCh37
NC_000017.9:g.6624774T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.863T>A MANE Select ENSP00000321386.4:p.Phe288Tyr
ENST00000321535.4:c.863T>A ENSP00000321386.4:p.Phe288Tyr
NM_153230.2:c.863T>A NP_694962.1:p.Phe288Tyr
XM_011523697.1:c.863T>A XP_011521999.1:p.Phe288Tyr
XR_243544.3:n.1041T>A
NM_153230.3:c.863T>A MANE Select NP_694962.1:p.Phe288Tyr
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