Canonical Allele Identifier: CA379629992

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9803061A>G (hg19) ; chr11:g.9781514A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781514A>G , CM000673.2:g.9781514A>G	GRCh38
NC_000011.9:g.9803061A>G , CM000673.1:g.9803061A>G	GRCh37
NC_000011.8:g.9759637A>G	NCBI36
NG_008074.1:g.517694T>C , LRG_267:g.517694T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1928T>C (SBF2)
ENST00000675281.2:c.5519T>C (SBF2)	ENSP00000502491.1:p.Phe1840Ser
ENST00000676324.2:c.*1752T>C (SBF2)	ENSP00000502578.1:n.*1752T>C
ENST00000676387.2:c.5501T>C (SBF2)	ENSP00000502779.1:p.Phe1834Ser
ENST00000688344.1:c.5051T>C (SBF2)	ENSP00000509987.1:p.Phe1684Ser
ENST00000689128.1:c.5540T>C (SBF2)	ENSP00000509587.1:p.Phe1847Ser
ENST00000689258.1:c.5381T>C (SBF2)	ENSP00000510475.1:p.Phe1794Ser
ENST00000689342.1:c.1610T>C (SBF2)
ENST00000689356.1:n.2615T>C (SBF2)
ENST00000689940.1:c.5438T>C (SBF2)	ENSP00000508452.1:p.Phe1813Ser
ENST00000690437.1:n.1393T>C (SBF2)
ENST00000690944.1:c.1524T>C (SBF2)
ENST00000691616.1:n.1920T>C (SBF2)
ENST00000692716.1:c.5315T>C (SBF2)	ENSP00000509545.1:p.Phe1772Ser
ENST00000693541.1:n.2363T>C (SBF2)
ENST00000256190.13:c.5444T>C (SBF2) MANE Select	ENSP00000256190.8:p.Phe1815Ser
ENST00000675281.1:c.5519T>C (SBF2)	ENSP00000502491.1:p.Phe1840Ser
ENST00000676324.1:c.*1752T>C (SBF2)	ENSP00000502578.1:n.*1752T>C
ENST00000676387.1:c.5501T>C (SBF2)	ENSP00000502779.1:p.Phe1834Ser
ENST00000256190.12:c.5444T>C (SBF2)	ENSP00000256190.8:p.Phe1815Ser
ENST00000525040.5:n.747T>C (SBF2)
ENST00000617179.4:c.5303T>C (SBF2)	ENSP00000482806.1:p.Phe1768Ser
NM_030962.3:c.5444T>C , LRG_267t1:c.5444T>C (SBF2)	NP_112224.1:p.Phe1815Ser
NR_036485.1:n.211+23011A>G (SBF2-AS1)
XM_005253154.3:c.5540T>C (SBF2)	XP_005253211.1:p.Phe1847Ser
XM_005253155.3:c.5411T>C (SBF2)	XP_005253212.1:p.Phe1804Ser
XM_011520394.1:c.5426T>C (SBF2)	XP_011518696.1:p.Phe1809Ser
XR_931024.1:n.200+939A>G
XR_931025.1:n.200+939A>G
XM_005253154.5:c.5540T>C (SBF2)	XP_005253211.1:p.Phe1847Ser
XM_005253155.5:c.5411T>C (SBF2)	XP_005253212.1:p.Phe1804Ser
XM_011520394.3:c.5426T>C (SBF2)	XP_011518696.1:p.Phe1809Ser
XM_017018372.2:c.5402T>C (SBF2)	XP_016873861.1:p.Phe1801Ser
XM_017018373.2:c.5402T>C (SBF2)	XP_016873862.1:p.Phe1801Ser
XM_017018374.2:c.5315T>C (SBF2)	XP_016873863.1:p.Phe1772Ser
XM_017018375.2:c.5303T>C (SBF2)	XP_016873864.1:p.Phe1768Ser
XR_001747994.2:n.5551T>C (SBF2)
XR_001748470.1:n.200+939A>G
XR_001748471.1:n.85+939A>G
NM_001386339.1:c.5540T>C (SBF2)	NP_001373268.1:p.Phe1847Ser
NM_001386342.1:c.5315T>C (SBF2)	NP_001373271.1:p.Phe1772Ser
NM_030962.4:c.5444T>C (SBF2) MANE Select	NP_112224.1:p.Phe1815Ser