Canonical Allele Identifier: CA2245514087
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1976502561
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780916C>T , CM000679.2:g.6780916C>T GRCh38
NC_000017.10:g.6684235C>T , CM000679.1:g.6684235C>T GRCh37
NC_000017.9:g.6624959C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1023+25C>T MANE Select ENSP00000321386.4:n.1023+25C>T
ENST00000321535.4:c.1023+25C>T ENSP00000321386.4:n.1023+25C>T
NM_153230.2:c.1023+25C>T NP_694962.1:n.1023+25C>T
XM_011523697.1:c.1023+25C>T XP_011521999.1:n.1023+25C>T
XR_243544.3:n.1201+25C>T
NM_153230.3:c.1023+25C>T MANE Select NP_694962.1:n.1023+25C>T
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