Canonical Allele Identifier: CA5880961

Gene: SBF2 SBF2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9795868T>C , CM000673.2:g.9795868T>C	GRCh38
NC_000011.9:g.9817415T>C , CM000673.1:g.9817415T>C	GRCh37
NC_000011.8:g.9773991T>C	NCBI36
NG_008074.1:g.503340A>G , LRG_267:g.503340A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1017A>G (SBF2)
ENST00000532095.2:n.1069A>G (SBF2)
ENST00000675281.2:c.4608A>G (SBF2)	ENSP00000502491.1:p.Thr1536=
ENST00000676324.2:c.*841A>G (SBF2)	ENSP00000502578.1:n.*841A>G
ENST00000676387.2:c.4590A>G (SBF2)	ENSP00000502779.1:p.Thr1530=
ENST00000688344.1:c.4140A>G (SBF2)	ENSP00000509987.1:p.Thr1380=
ENST00000689128.1:c.4629A>G (SBF2)	ENSP00000509587.1:p.Thr1543=
ENST00000689258.1:c.4470A>G (SBF2)	ENSP00000510475.1:p.Thr1490=
ENST00000689342.1:c.699A>G (SBF2)
ENST00000689356.1:n.1704A>G (SBF2)
ENST00000689597.1:c.3237A>G (SBF2)	ENSP00000510781.1:p.Thr1079=
ENST00000689940.1:c.4527A>G (SBF2)	ENSP00000508452.1:p.Thr1509=
ENST00000690944.1:c.651-5185A>G (SBF2)
ENST00000691616.1:n.1009A>G (SBF2)
ENST00000692716.1:c.4404A>G (SBF2)	ENSP00000509545.1:p.Thr1468=
ENST00000693541.1:n.1452A>G (SBF2)
ENST00000256190.13:c.4533A>G (SBF2) MANE Select	ENSP00000256190.8:p.Thr1511=
ENST00000675281.1:c.4608A>G (SBF2)	ENSP00000502491.1:p.Thr1536=
ENST00000676324.1:c.*841A>G (SBF2)	ENSP00000502578.1:n.*841A>G
ENST00000676387.1:c.4590A>G (SBF2)	ENSP00000502779.1:p.Thr1530=
ENST00000256190.12:c.4533A>G (SBF2)	ENSP00000256190.8:p.Thr1511=
ENST00000617179.4:c.4392A>G (SBF2)	ENSP00000482806.1:p.Thr1464=
NM_030962.3:c.4533A>G , LRG_267t1:c.4533A>G (SBF2)	NP_112224.1:p.Thr1511=
NR_036485.1:n.212-11980T>C (SBF2-AS1)
XM_005253154.3:c.4629A>G (SBF2)	XP_005253211.1:p.Thr1543=
XM_005253155.3:c.4500A>G (SBF2)	XP_005253212.1:p.Thr1500=
XM_011520394.1:c.4515A>G (SBF2)	XP_011518696.1:p.Thr1505=
XM_005253154.5:c.4629A>G (SBF2)	XP_005253211.1:p.Thr1543=
XM_005253155.5:c.4500A>G (SBF2)	XP_005253212.1:p.Thr1500=
XM_011520394.3:c.4515A>G (SBF2)	XP_011518696.1:p.Thr1505=
XM_017018372.2:c.4491A>G (SBF2)	XP_016873861.1:p.Thr1497=
XM_017018373.2:c.4491A>G (SBF2)	XP_016873862.1:p.Thr1497=
XM_017018374.2:c.4404A>G (SBF2)	XP_016873863.1:p.Thr1468=
XM_017018375.2:c.4392A>G (SBF2)	XP_016873864.1:p.Thr1464=
XR_001747994.2:n.4678-5185A>G (SBF2)
NM_001386339.1:c.4629A>G (SBF2)	NP_001373268.1:p.Thr1543=
NM_001386342.1:c.4404A>G (SBF2)	NP_001373271.1:p.Thr1468=
NM_030962.4:c.4533A>G (SBF2) MANE Select	NP_112224.1:p.Thr1511=