Canonical Allele Identifier: CA397761840
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683857C>T (hg19) chr17:g.6780538C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780538C>T , CM000679.2:g.6780538C>T GRCh38
NC_000017.10:g.6683857C>T , CM000679.1:g.6683857C>T GRCh37
NC_000017.9:g.6624581C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.670C>T MANE Select ENSP00000321386.4:p.His224Tyr
ENST00000321535.4:c.670C>T ENSP00000321386.4:p.His224Tyr
NM_153230.2:c.670C>T NP_694962.1:p.His224Tyr
XM_011523697.1:c.670C>T XP_011521999.1:p.His224Tyr
XR_243544.3:n.848C>T
NM_153230.3:c.670C>T MANE Select NP_694962.1:p.His224Tyr
Search 100 bp 5'
Search 100 bp 3'