Canonical Allele Identifier: CA2245513496
Gene: FBXO39 HGNC NCBI

Linked Data

dbSNP Id: rs1976494402
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780526_6780527del , CM000679.2:g.6780526_6780527del GRCh38
NC_000017.10:g.6683845_6683846del , CM000679.1:g.6683845_6683846del GRCh37
NC_000017.9:g.6624569_6624570del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.658_659del MANE Select ENSP00000321386.4:p.Met220ValfsTer22
ENST00000321535.4:c.658_659del ENSP00000321386.4:p.Met220ValfsTer22
NM_153230.2:c.658_659del NP_694962.1:p.Met220ValfsTer22
XM_011523697.1:c.658_659del XP_011521999.1:p.Met220ValfsTer22
XR_243544.3:n.836_837del
NM_153230.3:c.658_659del MANE Select NP_694962.1:p.Met220ValfsTer22
Search 100 bp 5'
Search 100 bp 3'