Canonical Allele Identifier: CA658822187

Gene: FBXO11

Linked Data

• ClinVar Variation Id: 559605
• ClinVar RCV Id: RCV000677382
• dbSNP Id: rs1553342101
• MyVariant Identifiers: chr2:g.48066557dup (hg19) ; chr2:g.47839418dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47839419dup , CM000664.2:g.47839419dup	GRCh38
NC_000002.11:g.48066558dup , CM000664.1:g.48066558dup	GRCh37
NC_000002.10:g.47920062dup	NCBI36
NG_008397.1:g.71258dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681999.1:n.319+1dup
ENST00000682451.1:n.291+1dup
ENST00000682975.1:n.337+1dup
ENST00000683894.1:c.190+1dup
ENST00000684085.1:n.319+1dup
ENST00000684712.1:n.550+1dup
ENST00000403359.8:c.442+1dup
ENST00000316377.8:c.208+1dup
ENST00000402508.5:c.190+1dup
ENST00000403359.7:c.442+1dup
ENST00000424163.2:c.190+1dup
ENST00000480038.1:n.405+1dup
ENST00000492225.5:n.290+1dup
NM_001190274.1:c.442+1dup
NM_025133.4:c.190+1dup
XM_005264572.3:c.442+1dup
XM_005264573.3:c.442+1dup
XM_005264572.5:c.442+1dup
XM_005264573.5:c.442+1dup
XM_017005015.1:c.442+1dup
XM_017005016.2:c.190+1dup
XM_017005017.1:c.190+1dup
NM_001190274.2:c.442+1dup
NM_001374325.1:c.190+1dup