Canonical Allele Identifier: CA1951768945

Gene: SBF2 SBF2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781509C= , CM000673.2:g.9781509C=	GRCh38
NC_000011.9:g.9803056C= , CM000673.1:g.9803056C=	GRCh37
NC_000011.8:g.9759632C=	NCBI36
NG_008074.1:g.517699G= , LRG_267:g.517699G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1933G= (SBF2)
ENST00000675281.2:c.5524G= (SBF2)	ENSP00000502491.1:p.Asp1842=
ENST00000676324.2:c.*1757G= (SBF2)	ENSP00000502578.1:n.*1757G=
ENST00000676387.2:c.5506G= (SBF2)	ENSP00000502779.1:p.Asp1836=
ENST00000688344.1:c.5056G= (SBF2)	ENSP00000509987.1:p.Asp1686=
ENST00000689128.1:c.5545G= (SBF2)	ENSP00000509587.1:p.Asp1849=
ENST00000689258.1:c.5386G= (SBF2)	ENSP00000510475.1:p.Asp1796=
ENST00000689342.1:c.1615G= (SBF2)
ENST00000689356.1:n.2620G= (SBF2)
ENST00000689940.1:c.5443G= (SBF2)	ENSP00000508452.1:p.Asp1815=
ENST00000690437.1:n.1398G= (SBF2)
ENST00000690944.1:c.1529G= (SBF2)
ENST00000691616.1:n.1925G= (SBF2)
ENST00000692716.1:c.5320G= (SBF2)	ENSP00000509545.1:p.Asp1774=
ENST00000693541.1:n.2368G= (SBF2)
ENST00000256190.13:c.5449G= (SBF2) MANE Select	ENSP00000256190.8:p.Asp1817=
ENST00000675281.1:c.5524G= (SBF2)	ENSP00000502491.1:p.Asp1842=
ENST00000676324.1:c.*1757G= (SBF2)	ENSP00000502578.1:n.*1757G=
ENST00000676387.1:c.5506G= (SBF2)	ENSP00000502779.1:p.Asp1836=
ENST00000256190.12:c.5449G= (SBF2)	ENSP00000256190.8:p.Asp1817=
ENST00000525040.5:n.752G= (SBF2)
ENST00000617179.4:c.5308G= (SBF2)	ENSP00000482806.1:p.Asp1770=
NM_030962.3:c.5449G= , LRG_267t1:c.5449G= (SBF2)	NP_112224.1:p.Asp1817=
NR_036485.1:n.211+23006C= (SBF2-AS1)
XM_005253154.3:c.5545G= (SBF2)	XP_005253211.1:p.Asp1849=
XM_005253155.3:c.5416G= (SBF2)	XP_005253212.1:p.Asp1806=
XM_011520394.1:c.5431G= (SBF2)	XP_011518696.1:p.Asp1811=
XR_931024.1:n.200+934C=
XR_931025.1:n.200+934C=
XM_005253154.5:c.5545G= (SBF2)	XP_005253211.1:p.Asp1849=
XM_005253155.5:c.5416G= (SBF2)	XP_005253212.1:p.Asp1806=
XM_011520394.3:c.5431G= (SBF2)	XP_011518696.1:p.Asp1811=
XM_017018372.2:c.5407G= (SBF2)	XP_016873861.1:p.Asp1803=
XM_017018373.2:c.5407G= (SBF2)	XP_016873862.1:p.Asp1803=
XM_017018374.2:c.5320G= (SBF2)	XP_016873863.1:p.Asp1774=
XM_017018375.2:c.5308G= (SBF2)	XP_016873864.1:p.Asp1770=
XR_001747994.2:n.5556G= (SBF2)
XR_001748470.1:n.200+934C=
XR_001748471.1:n.85+934C=
NM_001386339.1:c.5545G= (SBF2)	NP_001373268.1:p.Asp1849=
NM_001386342.1:c.5320G= (SBF2)	NP_001373271.1:p.Asp1774=
NM_030962.4:c.5449G= (SBF2) MANE Select	NP_112224.1:p.Asp1817=