Canonical Allele Identifier: CA379629979

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9803058A>G (hg19) ; chr11:g.9781511A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781511A>G , CM000673.2:g.9781511A>G	GRCh38
NC_000011.9:g.9803058A>G , CM000673.1:g.9803058A>G	GRCh37
NC_000011.8:g.9759634A>G	NCBI36
NG_008074.1:g.517697T>C , LRG_267:g.517697T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1931T>C (SBF2)
ENST00000675281.2:c.5522T>C (SBF2)	ENSP00000502491.1:p.Phe1841Ser
ENST00000676324.2:c.*1755T>C (SBF2)	ENSP00000502578.1:n.*1755T>C
ENST00000676387.2:c.5504T>C (SBF2)	ENSP00000502779.1:p.Phe1835Ser
ENST00000688344.1:c.5054T>C (SBF2)	ENSP00000509987.1:p.Phe1685Ser
ENST00000689128.1:c.5543T>C (SBF2)	ENSP00000509587.1:p.Phe1848Ser
ENST00000689258.1:c.5384T>C (SBF2)	ENSP00000510475.1:p.Phe1795Ser
ENST00000689342.1:c.1613T>C (SBF2)
ENST00000689356.1:n.2618T>C (SBF2)
ENST00000689940.1:c.5441T>C (SBF2)	ENSP00000508452.1:p.Phe1814Ser
ENST00000690437.1:n.1396T>C (SBF2)
ENST00000690944.1:c.1527T>C (SBF2)
ENST00000691616.1:n.1923T>C (SBF2)
ENST00000692716.1:c.5318T>C (SBF2)	ENSP00000509545.1:p.Phe1773Ser
ENST00000693541.1:n.2366T>C (SBF2)
ENST00000256190.13:c.5447T>C (SBF2) MANE Select	ENSP00000256190.8:p.Phe1816Ser
ENST00000675281.1:c.5522T>C (SBF2)	ENSP00000502491.1:p.Phe1841Ser
ENST00000676324.1:c.*1755T>C (SBF2)	ENSP00000502578.1:n.*1755T>C
ENST00000676387.1:c.5504T>C (SBF2)	ENSP00000502779.1:p.Phe1835Ser
ENST00000256190.12:c.5447T>C (SBF2)	ENSP00000256190.8:p.Phe1816Ser
ENST00000525040.5:n.750T>C (SBF2)
ENST00000617179.4:c.5306T>C (SBF2)	ENSP00000482806.1:p.Phe1769Ser
NM_030962.3:c.5447T>C , LRG_267t1:c.5447T>C (SBF2)	NP_112224.1:p.Phe1816Ser
NR_036485.1:n.211+23008A>G (SBF2-AS1)
XM_005253154.3:c.5543T>C (SBF2)	XP_005253211.1:p.Phe1848Ser
XM_005253155.3:c.5414T>C (SBF2)	XP_005253212.1:p.Phe1805Ser
XM_011520394.1:c.5429T>C (SBF2)	XP_011518696.1:p.Phe1810Ser
XR_931024.1:n.200+936A>G
XR_931025.1:n.200+936A>G
XM_005253154.5:c.5543T>C (SBF2)	XP_005253211.1:p.Phe1848Ser
XM_005253155.5:c.5414T>C (SBF2)	XP_005253212.1:p.Phe1805Ser
XM_011520394.3:c.5429T>C (SBF2)	XP_011518696.1:p.Phe1810Ser
XM_017018372.2:c.5405T>C (SBF2)	XP_016873861.1:p.Phe1802Ser
XM_017018373.2:c.5405T>C (SBF2)	XP_016873862.1:p.Phe1802Ser
XM_017018374.2:c.5318T>C (SBF2)	XP_016873863.1:p.Phe1773Ser
XM_017018375.2:c.5306T>C (SBF2)	XP_016873864.1:p.Phe1769Ser
XR_001747994.2:n.5554T>C (SBF2)
XR_001748470.1:n.200+936A>G
XR_001748471.1:n.85+936A>G
NM_001386339.1:c.5543T>C (SBF2)	NP_001373268.1:p.Phe1848Ser
NM_001386342.1:c.5318T>C (SBF2)	NP_001373271.1:p.Phe1773Ser
NM_030962.4:c.5447T>C (SBF2) MANE Select	NP_112224.1:p.Phe1816Ser