Canonical Allele Identifier: CA397762362
Gene: FBXO39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780682T>G , CM000679.2:g.6780682T>G GRCh38
NC_000017.10:g.6684001T>G , CM000679.1:g.6684001T>G GRCh37
NC_000017.9:g.6624725T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.814T>G MANE Select ENSP00000321386.4:p.Ser272Ala
ENST00000321535.4:c.814T>G ENSP00000321386.4:p.Ser272Ala
NM_153230.2:c.814T>G NP_694962.1:p.Ser272Ala
XM_011523697.1:c.814T>G XP_011521999.1:p.Ser272Ala
XR_243544.3:n.992T>G
NM_153230.3:c.814T>G MANE Select NP_694962.1:p.Ser272Ala