Canonical Allele Identifier: CA497596038
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6684126G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780807G>T , CM000679.2:g.6780807G>T GRCh38
NC_000017.10:g.6684126G>T , CM000679.1:g.6684126G>T GRCh37
NC_000017.9:g.6624850G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.939G>T MANE Select ENSP00000321386.4:p.Leu313=
ENST00000321535.4:c.939G>T ENSP00000321386.4:p.Leu313=
NM_153230.2:c.939G>T NP_694962.1:p.Leu313=
XM_011523697.1:c.939G>T XP_011521999.1:p.Leu313=
XR_243544.3:n.1117G>T
NM_153230.3:c.939G>T MANE Select NP_694962.1:p.Leu313=
Search 100 bp 5'
Search 100 bp 3'