Canonical Allele Identifier: CA497596028
Gene: FBXO39 HGNC NCBI

Linked Data

gnomAD v4: 17-6780792-C-T
MyVariant Identifiers: chr17:g.6684111C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780792C>T , CM000679.2:g.6780792C>T GRCh38
NC_000017.10:g.6684111C>T , CM000679.1:g.6684111C>T GRCh37
NC_000017.9:g.6624835C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.924C>T MANE Select ENSP00000321386.4:p.Ile308=
ENST00000321535.4:c.924C>T ENSP00000321386.4:p.Ile308=
NM_153230.2:c.924C>T NP_694962.1:p.Ile308=
XM_011523697.1:c.924C>T XP_011521999.1:p.Ile308=
XR_243544.3:n.1102C>T
NM_153230.3:c.924C>T MANE Select NP_694962.1:p.Ile308=
Search 100 bp 5'
Search 100 bp 3'