Canonical Allele Identifier: CA497690494
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684048C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780729C>T , CM000679.2:g.6780729C>T GRCh38
NC_000017.10:g.6684048C>T , CM000679.1:g.6684048C>T GRCh37
NC_000017.9:g.6624772C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.861C>T MANE Select ENSP00000321386.4:p.Phe287=
ENST00000321535.4:c.861C>T ENSP00000321386.4:p.Phe287=
NM_153230.2:c.861C>T NP_694962.1:p.Phe287=
XM_011523697.1:c.861C>T XP_011521999.1:p.Phe287=
XR_243544.3:n.1039C>T
NM_153230.3:c.861C>T MANE Select NP_694962.1:p.Phe287=
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