Canonical Allele Identifier: CA497690142
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683865T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780546T>G , CM000679.2:g.6780546T>G GRCh38
NC_000017.10:g.6683865T>G , CM000679.1:g.6683865T>G GRCh37
NC_000017.9:g.6624589T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.678T>G MANE Select ENSP00000321386.4:p.Leu226=
ENST00000321535.4:c.678T>G ENSP00000321386.4:p.Leu226=
NM_153230.2:c.678T>G NP_694962.1:p.Leu226=
XM_011523697.1:c.678T>G XP_011521999.1:p.Leu226=
XR_243544.3:n.856T>G
NM_153230.3:c.678T>G MANE Select NP_694962.1:p.Leu226=