Canonical Allele Identifier: CA379631795

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9806845T>G (hg19) ; chr11:g.9785298T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9785298T>G , CM000673.2:g.9785298T>G	GRCh38
NC_000011.9:g.9806845T>G , CM000673.1:g.9806845T>G	GRCh37
NC_000011.8:g.9763421T>G	NCBI36
NG_008074.1:g.513910A>C , LRG_267:g.513910A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1542A>C (SBF2)
ENST00000529587.2:n.52A>C (SBF2)
ENST00000532095.2:n.1594A>C (SBF2)
ENST00000675281.2:c.5133A>C (SBF2)	ENSP00000502491.1:p.Arg1711Ser
ENST00000676324.2:c.*1366A>C (SBF2)	ENSP00000502578.1:n.*1366A>C
ENST00000676387.2:c.5115A>C (SBF2)	ENSP00000502779.1:p.Arg1705Ser
ENST00000688344.1:c.4665A>C (SBF2)	ENSP00000509987.1:p.Arg1555Ser
ENST00000689128.1:c.5154A>C (SBF2)	ENSP00000509587.1:p.Arg1718Ser
ENST00000689258.1:c.4995A>C (SBF2)	ENSP00000510475.1:p.Arg1665Ser
ENST00000689342.1:c.1224A>C (SBF2)
ENST00000689356.1:n.2229A>C (SBF2)
ENST00000689597.1:c.3762A>C (SBF2)	ENSP00000510781.1:p.Arg1254Ser
ENST00000689940.1:c.5052A>C (SBF2)	ENSP00000508452.1:p.Arg1684Ser
ENST00000690944.1:c.1138A>C (SBF2)
ENST00000691616.1:n.1534A>C (SBF2)
ENST00000692716.1:c.4929A>C (SBF2)	ENSP00000509545.1:p.Arg1643Ser
ENST00000693541.1:n.1977A>C (SBF2)
ENST00000256190.13:c.5058A>C (SBF2) MANE Select	ENSP00000256190.8:p.Arg1686Ser
ENST00000675281.1:c.5133A>C (SBF2)	ENSP00000502491.1:p.Arg1711Ser
ENST00000676324.1:c.*1366A>C (SBF2)	ENSP00000502578.1:n.*1366A>C
ENST00000676387.1:c.5115A>C (SBF2)	ENSP00000502779.1:p.Arg1705Ser
ENST00000256190.12:c.5058A>C (SBF2)	ENSP00000256190.8:p.Arg1686Ser
ENST00000525040.5:n.361A>C (SBF2)
ENST00000529587.1:n.52A>C (SBF2)
ENST00000532095.1:c.222A>C (SBF2)	ENSP00000434620.1:p.Arg74Ser
ENST00000617179.4:c.4917A>C (SBF2)	ENSP00000482806.1:p.Arg1639Ser
NM_030962.3:c.5058A>C , LRG_267t1:c.5058A>C (SBF2)	NP_112224.1:p.Arg1686Ser
NR_036485.1:n.212-22550T>G (SBF2-AS1)
XM_005253154.3:c.5154A>C (SBF2)	XP_005253211.1:p.Arg1718Ser
XM_005253155.3:c.5025A>C (SBF2)	XP_005253212.1:p.Arg1675Ser
XM_011520394.1:c.5040A>C (SBF2)	XP_011518696.1:p.Arg1680Ser
XR_931024.1:n.455+522T>G
XR_931025.1:n.270+2189T>G
XM_005253154.5:c.5154A>C (SBF2)	XP_005253211.1:p.Arg1718Ser
XM_005253155.5:c.5025A>C (SBF2)	XP_005253212.1:p.Arg1675Ser
XM_011520394.3:c.5040A>C (SBF2)	XP_011518696.1:p.Arg1680Ser
XM_017018372.2:c.5016A>C (SBF2)	XP_016873861.1:p.Arg1672Ser
XM_017018373.2:c.5016A>C (SBF2)	XP_016873862.1:p.Arg1672Ser
XM_017018374.2:c.4929A>C (SBF2)	XP_016873863.1:p.Arg1643Ser
XM_017018375.2:c.4917A>C (SBF2)	XP_016873864.1:p.Arg1639Ser
XR_001747994.2:n.5165A>C (SBF2)
NM_001386339.1:c.5154A>C (SBF2)	NP_001373268.1:p.Arg1718Ser
NM_001386342.1:c.4929A>C (SBF2)	NP_001373271.1:p.Arg1643Ser
NM_030962.4:c.5058A>C (SBF2) MANE Select	NP_112224.1:p.Arg1686Ser