Canonical Allele Identifier: CA774339775
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1229499125
gnomAD v4: 17-6780682-TC-T
MyVariant Identifiers: chr17:g.6684002del (hg19) chr17:g.6780683del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780684del , CM000679.2:g.6780684del GRCh38
NC_000017.10:g.6684003del , CM000679.1:g.6684003del GRCh37
NC_000017.9:g.6624727del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.816del MANE Select ENSP00000321386.4:p.Trp273GlyfsTer11
ENST00000321535.4:c.816del ENSP00000321386.4:p.Trp273GlyfsTer11
NM_153230.2:c.816del NP_694962.1:p.Trp273GlyfsTer11
XM_011523697.1:c.816del XP_011521999.1:p.Trp273GlyfsTer11
XR_243544.3:n.994del
NM_153230.3:c.816del MANE Select NP_694962.1:p.Trp273GlyfsTer11
Search 100 bp 5'
Search 100 bp 3'