Canonical Allele Identifier: CA2635735036
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780919-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780919C>A , CM000679.2:g.6780919C>A GRCh38
NC_000017.10:g.6684238C>A , CM000679.1:g.6684238C>A GRCh37
NC_000017.9:g.6624962C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.1023+28C>A MANE Select ENSP00000321386.4:n.1023+28C>A
ENST00000321535.4:c.1023+28C>A ENSP00000321386.4:n.1023+28C>A
NM_153230.2:c.1023+28C>A NP_694962.1:n.1023+28C>A
XM_011523697.1:c.1023+28C>A XP_011521999.1:n.1023+28C>A
XR_243544.3:n.1201+28C>A
NM_153230.3:c.1023+28C>A MANE Select NP_694962.1:n.1023+28C>A
Search 100 bp 5'
Search 100 bp 3'