Canonical Allele Identifier: CA397762563
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684097C>A (hg19) chr17:g.6780778C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780778C>A , CM000679.2:g.6780778C>A GRCh38
NC_000017.10:g.6684097C>A , CM000679.1:g.6684097C>A GRCh37
NC_000017.9:g.6624821C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.910C>A MANE Select ENSP00000321386.4:p.Gln304Lys
ENST00000321535.4:c.910C>A ENSP00000321386.4:p.Gln304Lys
NM_153230.2:c.910C>A NP_694962.1:p.Gln304Lys
XM_011523697.1:c.910C>A XP_011521999.1:p.Gln304Lys
XR_243544.3:n.1088C>A
NM_153230.3:c.910C>A MANE Select NP_694962.1:p.Gln304Lys
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