Canonical Allele Identifier: CA397762454
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780725-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780725A>G , CM000679.2:g.6780725A>G GRCh38
NC_000017.10:g.6684044A>G , CM000679.1:g.6684044A>G GRCh37
NC_000017.9:g.6624768A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.857A>G MANE Select ENSP00000321386.4:p.Asn286Ser
ENST00000321535.4:c.857A>G ENSP00000321386.4:p.Asn286Ser
NM_153230.2:c.857A>G NP_694962.1:p.Asn286Ser
XM_011523697.1:c.857A>G XP_011521999.1:p.Asn286Ser
XR_243544.3:n.1035A>G
NM_153230.3:c.857A>G MANE Select NP_694962.1:p.Asn286Ser