Canonical Allele Identifier: CA497690146
Gene: FBXO39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6683868G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780549G>T , CM000679.2:g.6780549G>T GRCh38
NC_000017.10:g.6683868G>T , CM000679.1:g.6683868G>T GRCh37
NC_000017.9:g.6624592G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.681G>T MANE Select ENSP00000321386.4:p.Val227=
ENST00000321535.4:c.681G>T ENSP00000321386.4:p.Val227=
NM_153230.2:c.681G>T NP_694962.1:p.Val227=
XM_011523697.1:c.681G>T XP_011521999.1:p.Val227=
XR_243544.3:n.859G>T
NM_153230.3:c.681G>T MANE Select NP_694962.1:p.Val227=