Canonical Allele Identifier: CA8332540
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs750170907
gnomAD v2: 17-6684219-G-A
gnomAD v4: 17-6780900-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780900G>A , CM000679.2:g.6780900G>A GRCh38
NC_000017.10:g.6684219G>A , CM000679.1:g.6684219G>A GRCh37
NC_000017.9:g.6624943G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1023+9G>A MANE Select ENSP00000321386.4:n.1023+9G>A
ENST00000321535.4:c.1023+9G>A ENSP00000321386.4:n.1023+9G>A
NM_153230.2:c.1023+9G>A NP_694962.1:n.1023+9G>A
XM_011523697.1:c.1023+9G>A XP_011521999.1:n.1023+9G>A
XR_243544.3:n.1201+9G>A
NM_153230.3:c.1023+9G>A MANE Select NP_694962.1:n.1023+9G>A