Canonical Allele Identifier: CA1951768949

Gene: SBF2 SBF2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781510A= , CM000673.2:g.9781510A=	GRCh38
NC_000011.9:g.9803057A= , CM000673.1:g.9803057A=	GRCh37
NC_000011.8:g.9759633A=	NCBI36
NG_008074.1:g.517698T= , LRG_267:g.517698T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1932T= (SBF2)
ENST00000675281.2:c.5523T= (SBF2)	ENSP00000502491.1:p.Phe1841=
ENST00000676324.2:c.*1756T= (SBF2)	ENSP00000502578.1:n.*1756T=
ENST00000676387.2:c.5505T= (SBF2)	ENSP00000502779.1:p.Phe1835=
ENST00000688344.1:c.5055T= (SBF2)	ENSP00000509987.1:p.Phe1685=
ENST00000689128.1:c.5544T= (SBF2)	ENSP00000509587.1:p.Phe1848=
ENST00000689258.1:c.5385T= (SBF2)	ENSP00000510475.1:p.Phe1795=
ENST00000689342.1:c.1614T= (SBF2)
ENST00000689356.1:n.2619T= (SBF2)
ENST00000689940.1:c.5442T= (SBF2)	ENSP00000508452.1:p.Phe1814=
ENST00000690437.1:n.1397T= (SBF2)
ENST00000690944.1:c.1528T= (SBF2)
ENST00000691616.1:n.1924T= (SBF2)
ENST00000692716.1:c.5319T= (SBF2)	ENSP00000509545.1:p.Phe1773=
ENST00000693541.1:n.2367T= (SBF2)
ENST00000256190.13:c.5448T= (SBF2) MANE Select	ENSP00000256190.8:p.Phe1816=
ENST00000675281.1:c.5523T= (SBF2)	ENSP00000502491.1:p.Phe1841=
ENST00000676324.1:c.*1756T= (SBF2)	ENSP00000502578.1:n.*1756T=
ENST00000676387.1:c.5505T= (SBF2)	ENSP00000502779.1:p.Phe1835=
ENST00000256190.12:c.5448T= (SBF2)	ENSP00000256190.8:p.Phe1816=
ENST00000525040.5:n.751T= (SBF2)
ENST00000617179.4:c.5307T= (SBF2)	ENSP00000482806.1:p.Phe1769=
NM_030962.3:c.5448T= , LRG_267t1:c.5448T= (SBF2)	NP_112224.1:p.Phe1816=
NR_036485.1:n.211+23007A= (SBF2-AS1)
XM_005253154.3:c.5544T= (SBF2)	XP_005253211.1:p.Phe1848=
XM_005253155.3:c.5415T= (SBF2)	XP_005253212.1:p.Phe1805=
XM_011520394.1:c.5430T= (SBF2)	XP_011518696.1:p.Phe1810=
XR_931024.1:n.200+935A=
XR_931025.1:n.200+935A=
XM_005253154.5:c.5544T= (SBF2)	XP_005253211.1:p.Phe1848=
XM_005253155.5:c.5415T= (SBF2)	XP_005253212.1:p.Phe1805=
XM_011520394.3:c.5430T= (SBF2)	XP_011518696.1:p.Phe1810=
XM_017018372.2:c.5406T= (SBF2)	XP_016873861.1:p.Phe1802=
XM_017018373.2:c.5406T= (SBF2)	XP_016873862.1:p.Phe1802=
XM_017018374.2:c.5319T= (SBF2)	XP_016873863.1:p.Phe1773=
XM_017018375.2:c.5307T= (SBF2)	XP_016873864.1:p.Phe1769=
XR_001747994.2:n.5555T= (SBF2)
XR_001748470.1:n.200+935A=
XR_001748471.1:n.85+935A=
NM_001386339.1:c.5544T= (SBF2)	NP_001373268.1:p.Phe1848=
NM_001386342.1:c.5319T= (SBF2)	NP_001373271.1:p.Phe1773=
NM_030962.4:c.5448T= (SBF2) MANE Select	NP_112224.1:p.Phe1816=