Canonical Allele Identifier: CA346813373
Gene: FBXO11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.48066586T>G (hg19) chr2:g.47839447T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47839447T>G , CM000664.2:g.47839447T>G GRCh38
NC_000002.11:g.48066586T>G , CM000664.1:g.48066586T>G GRCh37
NC_000002.10:g.47920090T>G NCBI36
NG_008397.1:g.71229A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000681999.1:n.291A>C
ENST00000682451.1:n.263A>C
ENST00000682975.1:n.309A>C
ENST00000683894.1:c.162A>C ENSP00000507789.1:p.Arg54Ser
ENST00000684085.1:n.291A>C
ENST00000684712.1:n.522A>C
ENST00000403359.8:c.414A>C MANE Select ENSP00000384823.4:p.Arg138Ser
ENST00000316377.8:c.182A>C ENSP00000323822.5:p.Glu61Ala
ENST00000402508.5:c.162A>C ENSP00000385398.1:p.Arg54Ser
ENST00000403359.7:c.414A>C ENSP00000384823.3:p.Arg138Ser
ENST00000424163.2:c.162A>C ENSP00000392272.1:p.Arg54Ser
ENST00000480038.1:n.377A>C
ENST00000492225.5:n.262A>C
NM_001190274.1:c.414A>C NP_001177203.1:p.Arg138Ser
NM_025133.4:c.162A>C NP_079409.3:p.Arg54Ser
XM_005264572.3:c.414A>C XP_005264629.1:p.Arg138Ser
XM_005264573.3:c.414A>C XP_005264630.1:p.Arg138Ser
XM_005264572.5:c.414A>C XP_005264629.1:p.Arg138Ser
XM_005264573.5:c.414A>C XP_005264630.1:p.Arg138Ser
XM_017005015.1:c.414A>C XP_016860504.1:p.Arg138Ser
XM_017005016.2:c.162A>C XP_016860505.1:p.Arg54Ser
XM_017005017.1:c.162A>C XP_016860506.1:p.Arg54Ser
NM_001190274.2:c.414A>C MANE Select NP_001177203.1:p.Arg138Ser
NM_001374325.1:c.162A>C NP_001361254.1:p.Arg54Ser
Search 100 bp 5'
Search 100 bp 3'