Canonical Allele Identifier: CA397761474
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1288183802
gnomAD v4: 17-6780475-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780475T>C , CM000679.2:g.6780475T>C GRCh38
NC_000017.10:g.6683794T>C , CM000679.1:g.6683794T>C GRCh37
NC_000017.9:g.6624518T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.607T>C MANE Select ENSP00000321386.4:p.Tyr203His
ENST00000321535.4:c.607T>C ENSP00000321386.4:p.Tyr203His
NM_153230.2:c.607T>C NP_694962.1:p.Tyr203His
XM_011523697.1:c.607T>C XP_011521999.1:p.Tyr203His
XR_243544.3:n.785T>C
NM_153230.3:c.607T>C MANE Select NP_694962.1:p.Tyr203His