Canonical Allele Identifier: CA497596025
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs764013991
gnomAD v2: 17-6684108-G-A
gnomAD v3: 17-6780789-G-A
gnomAD v4: 17-6780789-G-A
COSMIC: COSM179543
MyVariant Identifiers: chr17:g.6684108G>A (hg19) chr17:g.6780789G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780789G>A , CM000679.2:g.6780789G>A GRCh38
NC_000017.10:g.6684108G>A , CM000679.1:g.6684108G>A GRCh37
NC_000017.9:g.6624832G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.921G>A MANE Select ENSP00000321386.4:p.Pro307=
ENST00000321535.4:c.921G>A ENSP00000321386.4:p.Pro307=
NM_153230.2:c.921G>A NP_694962.1:p.Pro307=
XM_011523697.1:c.921G>A XP_011521999.1:p.Pro307=
XR_243544.3:n.1099G>A
NM_153230.3:c.921G>A MANE Select NP_694962.1:p.Pro307=
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