Canonical Allele Identifier: CA397761822
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683854T>G (hg19) chr17:g.6780535T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780535T>G , CM000679.2:g.6780535T>G GRCh38
NC_000017.10:g.6683854T>G , CM000679.1:g.6683854T>G GRCh37
NC_000017.9:g.6624578T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.667T>G MANE Select ENSP00000321386.4:p.Phe223Val
ENST00000321535.4:c.667T>G ENSP00000321386.4:p.Phe223Val
NM_153230.2:c.667T>G NP_694962.1:p.Phe223Val
XM_011523697.1:c.667T>G XP_011521999.1:p.Phe223Val
XR_243544.3:n.845T>G
NM_153230.3:c.667T>G MANE Select NP_694962.1:p.Phe223Val
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