Canonical Allele Identifier: CA2635735021
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780904-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780904T>C , CM000679.2:g.6780904T>C GRCh38
NC_000017.10:g.6684223T>C , CM000679.1:g.6684223T>C GRCh37
NC_000017.9:g.6624947T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1023+13T>C MANE Select ENSP00000321386.4:n.1023+13T>C
ENST00000321535.4:c.1023+13T>C ENSP00000321386.4:n.1023+13T>C
NM_153230.2:c.1023+13T>C NP_694962.1:n.1023+13T>C
XM_011523697.1:c.1023+13T>C XP_011521999.1:n.1023+13T>C
XR_243544.3:n.1201+13T>C
NM_153230.3:c.1023+13T>C MANE Select NP_694962.1:n.1023+13T>C
Search 100 bp 5'
Search 100 bp 3'