Canonical Allele Identifier: CA2245513930
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1976500028
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780799_6780800del , CM000679.2:g.6780799_6780800del GRCh38
NC_000017.10:g.6684118_6684119del , CM000679.1:g.6684118_6684119del GRCh37
NC_000017.9:g.6624842_6624843del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.931_932del MANE Select ENSP00000321386.4:p.Ile311GlnfsTer9
ENST00000321535.4:c.931_932del ENSP00000321386.4:p.Ile311GlnfsTer9
NM_153230.2:c.931_932del NP_694962.1:p.Ile311GlnfsTer9
XM_011523697.1:c.931_932del XP_011521999.1:p.Ile311GlnfsTer9
XR_243544.3:n.1109_1110del
NM_153230.3:c.931_932del MANE Select NP_694962.1:p.Ile311GlnfsTer9
Search 100 bp 5'
Search 100 bp 3'