Canonical Allele Identifier: CA473053855

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9803165A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781618A>T , CM000673.2:g.9781618A>T	GRCh38
NC_000011.9:g.9803165A>T , CM000673.1:g.9803165A>T	GRCh37
NC_000011.8:g.9759741A>T	NCBI36
NG_008074.1:g.517590T>A , LRG_267:g.517590T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1824T>A (SBF2)
ENST00000529587.2:n.334T>A (SBF2)
ENST00000675281.2:c.5415T>A (SBF2)	ENSP00000502491.1:p.Gly1805=
ENST00000676324.2:c.*1648T>A (SBF2)	ENSP00000502578.1:n.*1648T>A
ENST00000676387.2:c.5397T>A (SBF2)	ENSP00000502779.1:p.Gly1799=
ENST00000688344.1:c.4947T>A (SBF2)	ENSP00000509987.1:p.Gly1649=
ENST00000689128.1:c.5436T>A (SBF2)	ENSP00000509587.1:p.Gly1812=
ENST00000689258.1:c.5277T>A (SBF2)	ENSP00000510475.1:p.Gly1759=
ENST00000689342.1:c.1506T>A (SBF2)
ENST00000689356.1:n.2511T>A (SBF2)
ENST00000689940.1:c.5334T>A (SBF2)	ENSP00000508452.1:p.Gly1778=
ENST00000690437.1:n.1289T>A (SBF2)
ENST00000690944.1:c.1420T>A (SBF2)
ENST00000691616.1:n.1816T>A (SBF2)
ENST00000692716.1:c.5211T>A (SBF2)	ENSP00000509545.1:p.Gly1737=
ENST00000693541.1:n.2259T>A (SBF2)
ENST00000256190.13:c.5340T>A (SBF2) MANE Select	ENSP00000256190.8:p.Gly1780=
ENST00000675281.1:c.5415T>A (SBF2)	ENSP00000502491.1:p.Gly1805=
ENST00000676324.1:c.*1648T>A (SBF2)	ENSP00000502578.1:n.*1648T>A
ENST00000676387.1:c.5397T>A (SBF2)	ENSP00000502779.1:p.Gly1799=
ENST00000256190.12:c.5340T>A (SBF2)	ENSP00000256190.8:p.Gly1780=
ENST00000525040.5:n.643T>A (SBF2)
ENST00000529587.1:n.334T>A (SBF2)
ENST00000617179.4:c.5199T>A (SBF2)	ENSP00000482806.1:p.Gly1733=
NM_030962.3:c.5340T>A , LRG_267t1:c.5340T>A (SBF2)	NP_112224.1:p.Gly1780=
NR_036485.1:n.211+23115A>T (SBF2-AS1)
XM_005253154.3:c.5436T>A (SBF2)	XP_005253211.1:p.Gly1812=
XM_005253155.3:c.5307T>A (SBF2)	XP_005253212.1:p.Gly1769=
XM_011520394.1:c.5322T>A (SBF2)	XP_011518696.1:p.Gly1774=
XR_931024.1:n.200+1043A>T
XR_931025.1:n.200+1043A>T
XM_005253154.5:c.5436T>A (SBF2)	XP_005253211.1:p.Gly1812=
XM_005253155.5:c.5307T>A (SBF2)	XP_005253212.1:p.Gly1769=
XM_011520394.3:c.5322T>A (SBF2)	XP_011518696.1:p.Gly1774=
XM_017018372.2:c.5298T>A (SBF2)	XP_016873861.1:p.Gly1766=
XM_017018373.2:c.5298T>A (SBF2)	XP_016873862.1:p.Gly1766=
XM_017018374.2:c.5211T>A (SBF2)	XP_016873863.1:p.Gly1737=
XM_017018375.2:c.5199T>A (SBF2)	XP_016873864.1:p.Gly1733=
XR_001747994.2:n.5447T>A (SBF2)
XR_001748470.1:n.200+1043A>T
XR_001748471.1:n.85+1043A>T
NM_001386339.1:c.5436T>A (SBF2)	NP_001373268.1:p.Gly1812=
NM_001386342.1:c.5211T>A (SBF2)	NP_001373271.1:p.Gly1737=
NM_030962.4:c.5340T>A (SBF2) MANE Select	NP_112224.1:p.Gly1780=