Canonical Allele Identifier: CA379631496

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9806701G>T (hg19) ; chr11:g.9785154G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9785154G>T , CM000673.2:g.9785154G>T	GRCh38
NC_000011.9:g.9806701G>T , CM000673.1:g.9806701G>T	GRCh37
NC_000011.8:g.9763277G>T	NCBI36
NG_008074.1:g.514054C>A , LRG_267:g.514054C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1686C>A (SBF2)
ENST00000529587.2:n.196C>A (SBF2)
ENST00000532095.2:n.1738C>A (SBF2)
ENST00000675281.2:c.5277C>A (SBF2)	ENSP00000502491.1:p.Ser1759Arg
ENST00000676324.2:c.*1510C>A (SBF2)	ENSP00000502578.1:n.*1510C>A
ENST00000676387.2:c.5259C>A (SBF2)	ENSP00000502779.1:p.Ser1753Arg
ENST00000688344.1:c.4809C>A (SBF2)	ENSP00000509987.1:p.Ser1603Arg
ENST00000689128.1:c.5298C>A (SBF2)	ENSP00000509587.1:p.Ser1766Arg
ENST00000689258.1:c.5139C>A (SBF2)	ENSP00000510475.1:p.Ser1713Arg
ENST00000689342.1:c.1368C>A (SBF2)
ENST00000689356.1:n.2373C>A (SBF2)
ENST00000689597.1:c.3906C>A (SBF2)	ENSP00000510781.1:p.Ser1302Arg
ENST00000689940.1:c.5196C>A (SBF2)	ENSP00000508452.1:p.Ser1732Arg
ENST00000690944.1:c.1282C>A (SBF2)
ENST00000691616.1:n.1678C>A (SBF2)
ENST00000692716.1:c.5073C>A (SBF2)	ENSP00000509545.1:p.Ser1691Arg
ENST00000693541.1:n.2121C>A (SBF2)
ENST00000256190.13:c.5202C>A (SBF2) MANE Select	ENSP00000256190.8:p.Ser1734Arg
ENST00000675281.1:c.5277C>A (SBF2)	ENSP00000502491.1:p.Ser1759Arg
ENST00000676324.1:c.*1510C>A (SBF2)	ENSP00000502578.1:n.*1510C>A
ENST00000676387.1:c.5259C>A (SBF2)	ENSP00000502779.1:p.Ser1753Arg
ENST00000256190.12:c.5202C>A (SBF2)	ENSP00000256190.8:p.Ser1734Arg
ENST00000525040.5:n.505C>A (SBF2)
ENST00000529587.1:n.196C>A (SBF2)
ENST00000532095.1:c.366C>A (SBF2)	ENSP00000434620.1:p.Ser122Arg
ENST00000617179.4:c.5061C>A (SBF2)	ENSP00000482806.1:p.Ser1687Arg
NM_030962.3:c.5202C>A , LRG_267t1:c.5202C>A (SBF2)	NP_112224.1:p.Ser1734Arg
NR_036485.1:n.212-22694G>T (SBF2-AS1)
XM_005253154.3:c.5298C>A (SBF2)	XP_005253211.1:p.Ser1766Arg
XM_005253155.3:c.5169C>A (SBF2)	XP_005253212.1:p.Ser1723Arg
XM_011520394.1:c.5184C>A (SBF2)	XP_011518696.1:p.Ser1728Arg
XR_931024.1:n.455+378G>T
XR_931025.1:n.270+2045G>T
XM_005253154.5:c.5298C>A (SBF2)	XP_005253211.1:p.Ser1766Arg
XM_005253155.5:c.5169C>A (SBF2)	XP_005253212.1:p.Ser1723Arg
XM_011520394.3:c.5184C>A (SBF2)	XP_011518696.1:p.Ser1728Arg
XM_017018372.2:c.5160C>A (SBF2)	XP_016873861.1:p.Ser1720Arg
XM_017018373.2:c.5160C>A (SBF2)	XP_016873862.1:p.Ser1720Arg
XM_017018374.2:c.5073C>A (SBF2)	XP_016873863.1:p.Ser1691Arg
XM_017018375.2:c.5061C>A (SBF2)	XP_016873864.1:p.Ser1687Arg
XR_001747994.2:n.5309C>A (SBF2)
NM_001386339.1:c.5298C>A (SBF2)	NP_001373268.1:p.Ser1766Arg
NM_001386342.1:c.5073C>A (SBF2)	NP_001373271.1:p.Ser1691Arg
NM_030962.4:c.5202C>A (SBF2) MANE Select	NP_112224.1:p.Ser1734Arg