Canonical Allele Identifier: CA379629982

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9803059A>C (hg19) ; chr11:g.9781512A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781512A>C , CM000673.2:g.9781512A>C	GRCh38
NC_000011.9:g.9803059A>C , CM000673.1:g.9803059A>C	GRCh37
NC_000011.8:g.9759635A>C	NCBI36
NG_008074.1:g.517696T>G , LRG_267:g.517696T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1930T>G (SBF2)
ENST00000675281.2:c.5521T>G (SBF2)	ENSP00000502491.1:p.Phe1841Val
ENST00000676324.2:c.*1754T>G (SBF2)	ENSP00000502578.1:n.*1754T>G
ENST00000676387.2:c.5503T>G (SBF2)	ENSP00000502779.1:p.Phe1835Val
ENST00000688344.1:c.5053T>G (SBF2)	ENSP00000509987.1:p.Phe1685Val
ENST00000689128.1:c.5542T>G (SBF2)	ENSP00000509587.1:p.Phe1848Val
ENST00000689258.1:c.5383T>G (SBF2)	ENSP00000510475.1:p.Phe1795Val
ENST00000689342.1:c.1612T>G (SBF2)
ENST00000689356.1:n.2617T>G (SBF2)
ENST00000689940.1:c.5440T>G (SBF2)	ENSP00000508452.1:p.Phe1814Val
ENST00000690437.1:n.1395T>G (SBF2)
ENST00000690944.1:c.1526T>G (SBF2)
ENST00000691616.1:n.1922T>G (SBF2)
ENST00000692716.1:c.5317T>G (SBF2)	ENSP00000509545.1:p.Phe1773Val
ENST00000693541.1:n.2365T>G (SBF2)
ENST00000256190.13:c.5446T>G (SBF2) MANE Select	ENSP00000256190.8:p.Phe1816Val
ENST00000675281.1:c.5521T>G (SBF2)	ENSP00000502491.1:p.Phe1841Val
ENST00000676324.1:c.*1754T>G (SBF2)	ENSP00000502578.1:n.*1754T>G
ENST00000676387.1:c.5503T>G (SBF2)	ENSP00000502779.1:p.Phe1835Val
ENST00000256190.12:c.5446T>G (SBF2)	ENSP00000256190.8:p.Phe1816Val
ENST00000525040.5:n.749T>G (SBF2)
ENST00000617179.4:c.5305T>G (SBF2)	ENSP00000482806.1:p.Phe1769Val
NM_030962.3:c.5446T>G , LRG_267t1:c.5446T>G (SBF2)	NP_112224.1:p.Phe1816Val
NR_036485.1:n.211+23009A>C (SBF2-AS1)
XM_005253154.3:c.5542T>G (SBF2)	XP_005253211.1:p.Phe1848Val
XM_005253155.3:c.5413T>G (SBF2)	XP_005253212.1:p.Phe1805Val
XM_011520394.1:c.5428T>G (SBF2)	XP_011518696.1:p.Phe1810Val
XR_931024.1:n.200+937A>C
XR_931025.1:n.200+937A>C
XM_005253154.5:c.5542T>G (SBF2)	XP_005253211.1:p.Phe1848Val
XM_005253155.5:c.5413T>G (SBF2)	XP_005253212.1:p.Phe1805Val
XM_011520394.3:c.5428T>G (SBF2)	XP_011518696.1:p.Phe1810Val
XM_017018372.2:c.5404T>G (SBF2)	XP_016873861.1:p.Phe1802Val
XM_017018373.2:c.5404T>G (SBF2)	XP_016873862.1:p.Phe1802Val
XM_017018374.2:c.5317T>G (SBF2)	XP_016873863.1:p.Phe1773Val
XM_017018375.2:c.5305T>G (SBF2)	XP_016873864.1:p.Phe1769Val
XR_001747994.2:n.5553T>G (SBF2)
XR_001748470.1:n.200+937A>C
XR_001748471.1:n.85+937A>C
NM_001386339.1:c.5542T>G (SBF2)	NP_001373268.1:p.Phe1848Val
NM_001386342.1:c.5317T>G (SBF2)	NP_001373271.1:p.Phe1773Val
NM_030962.4:c.5446T>G (SBF2) MANE Select	NP_112224.1:p.Phe1816Val