Canonical Allele Identifier: CA2245513737
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780678T= , CM000679.2:g.6780678T= GRCh38
NC_000017.10:g.6683997T= , CM000679.1:g.6683997T= GRCh37
NC_000017.9:g.6624721T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.810T= MANE Select ENSP00000321386.4:p.Gly270=
ENST00000321535.4:c.810T= ENSP00000321386.4:p.Gly270=
NM_153230.2:c.810T= NP_694962.1:p.Gly270=
XM_011523697.1:c.810T= XP_011521999.1:p.Gly270=
XR_243544.3:n.988T=
NM_153230.3:c.810T= MANE Select NP_694962.1:p.Gly270=