Canonical Allele Identifier: CA397761435
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683789A>T (hg19) chr17:g.6780470A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780470A>T , CM000679.2:g.6780470A>T GRCh38
NC_000017.10:g.6683789A>T , CM000679.1:g.6683789A>T GRCh37
NC_000017.9:g.6624513A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.602A>T MANE Select ENSP00000321386.4:p.Glu201Val
ENST00000321535.4:c.602A>T ENSP00000321386.4:p.Glu201Val
NM_153230.2:c.602A>T NP_694962.1:p.Glu201Val
XM_011523697.1:c.602A>T XP_011521999.1:p.Glu201Val
XR_243544.3:n.780A>T
NM_153230.3:c.602A>T MANE Select NP_694962.1:p.Glu201Val
Search 100 bp 5'
Search 100 bp 3'