Canonical Allele Identifier: CA1649821

Gene: FBXO11

Linked Data

• dbSNP Id: rs770803012
• ExAC: 2:48050305 G / A
• gnomAD v2: 2-48050305-G-A
• gnomAD v3: 2-47823166-G-A
• gnomAD v4: 2-47823166-G-A
• MyVariant Identifiers: chr2:g.48050305G>A (hg19) ; chr2:g.47823166G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47823166G>A , CM000664.2:g.47823166G>A	GRCh38
NC_000002.11:g.48050305G>A , CM000664.1:g.48050305G>A	GRCh37
NC_000002.10:g.47903809G>A	NCBI36
NG_008397.1:g.87510C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681999.1:n.1470C>T
ENST00000682451.1:n.1439C>T
ENST00000682975.1:n.1488C>T
ENST00000683894.1:c.1341C>T	ENSP00000507789.1:p.Thr447=
ENST00000684085.1:n.1470C>T
ENST00000684712.1:n.1701C>T
ENST00000403359.8:c.1593C>T MANE Select	ENSP00000384823.4:p.Thr531=
ENST00000316377.8:c.1359C>T	ENSP00000323822.5:p.Thr453=
ENST00000402508.5:c.1341C>T	ENSP00000385398.1:p.Thr447=
ENST00000403359.7:c.1593C>T	ENSP00000384823.3:p.Thr531=
ENST00000492225.5:n.1441C>T
ENST00000493962.6:c.967C>T
NM_001190274.1:c.1593C>T	NP_001177203.1:p.Thr531=
NM_025133.4:c.1341C>T	NP_079409.3:p.Thr447=
XM_005264572.3:c.1593C>T	XP_005264629.1:p.Thr531=
XM_005264573.3:c.1590C>T	XP_005264630.1:p.Thr530=
XM_005264572.5:c.1593C>T	XP_005264629.1:p.Thr531=
XM_005264573.5:c.1590C>T	XP_005264630.1:p.Thr530=
XM_017005015.1:c.1590C>T	XP_016860504.1:p.Thr530=
XM_017005016.2:c.1341C>T	XP_016860505.1:p.Thr447=
XM_017005017.1:c.1341C>T	XP_016860506.1:p.Thr447=
NM_001190274.2:c.1593C>T MANE Select	NP_001177203.1:p.Thr531=
NM_001374325.1:c.1341C>T	NP_001361254.1:p.Thr447=