Canonical Allele Identifier: CA397761731
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683837A>T (hg19) chr17:g.6780518A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780518A>T , CM000679.2:g.6780518A>T GRCh38
NC_000017.10:g.6683837A>T , CM000679.1:g.6683837A>T GRCh37
NC_000017.9:g.6624561A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.650A>T MANE Select ENSP00000321386.4:p.Lys217Ile
ENST00000321535.4:c.650A>T ENSP00000321386.4:p.Lys217Ile
NM_153230.2:c.650A>T NP_694962.1:p.Lys217Ile
XM_011523697.1:c.650A>T XP_011521999.1:p.Lys217Ile
XR_243544.3:n.828A>T
NM_153230.3:c.650A>T MANE Select NP_694962.1:p.Lys217Ile
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