Canonical Allele Identifier: CA379629967

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9803055T>G (hg19) ; chr11:g.9781508T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781508T>G , CM000673.2:g.9781508T>G	GRCh38
NC_000011.9:g.9803055T>G , CM000673.1:g.9803055T>G	GRCh37
NC_000011.8:g.9759631T>G	NCBI36
NG_008074.1:g.517700A>C , LRG_267:g.517700A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1934A>C (SBF2)
ENST00000675281.2:c.5525A>C (SBF2)	ENSP00000502491.1:p.Asp1842Ala
ENST00000676324.2:c.*1758A>C (SBF2)	ENSP00000502578.1:n.*1758A>C
ENST00000676387.2:c.5507A>C (SBF2)	ENSP00000502779.1:p.Asp1836Ala
ENST00000688344.1:c.5057A>C (SBF2)	ENSP00000509987.1:p.Asp1686Ala
ENST00000689128.1:c.5546A>C (SBF2)	ENSP00000509587.1:p.Asp1849Ala
ENST00000689258.1:c.5387A>C (SBF2)	ENSP00000510475.1:p.Asp1796Ala
ENST00000689342.1:c.1616A>C (SBF2)
ENST00000689356.1:n.2621A>C (SBF2)
ENST00000689940.1:c.5444A>C (SBF2)	ENSP00000508452.1:p.Asp1815Ala
ENST00000690437.1:n.1399A>C (SBF2)
ENST00000690944.1:c.1530A>C (SBF2)
ENST00000691616.1:n.1926A>C (SBF2)
ENST00000692716.1:c.5321A>C (SBF2)	ENSP00000509545.1:p.Asp1774Ala
ENST00000693541.1:n.2369A>C (SBF2)
ENST00000256190.13:c.5450A>C (SBF2) MANE Select	ENSP00000256190.8:p.Asp1817Ala
ENST00000675281.1:c.5525A>C (SBF2)	ENSP00000502491.1:p.Asp1842Ala
ENST00000676324.1:c.*1758A>C (SBF2)	ENSP00000502578.1:n.*1758A>C
ENST00000676387.1:c.5507A>C (SBF2)	ENSP00000502779.1:p.Asp1836Ala
ENST00000256190.12:c.5450A>C (SBF2)	ENSP00000256190.8:p.Asp1817Ala
ENST00000525040.5:n.753A>C (SBF2)
ENST00000617179.4:c.5309A>C (SBF2)	ENSP00000482806.1:p.Asp1770Ala
NM_030962.3:c.5450A>C , LRG_267t1:c.5450A>C (SBF2)	NP_112224.1:p.Asp1817Ala
NR_036485.1:n.211+23005T>G (SBF2-AS1)
XM_005253154.3:c.5546A>C (SBF2)	XP_005253211.1:p.Asp1849Ala
XM_005253155.3:c.5417A>C (SBF2)	XP_005253212.1:p.Asp1806Ala
XM_011520394.1:c.5432A>C (SBF2)	XP_011518696.1:p.Asp1811Ala
XR_931024.1:n.200+933T>G
XR_931025.1:n.200+933T>G
XM_005253154.5:c.5546A>C (SBF2)	XP_005253211.1:p.Asp1849Ala
XM_005253155.5:c.5417A>C (SBF2)	XP_005253212.1:p.Asp1806Ala
XM_011520394.3:c.5432A>C (SBF2)	XP_011518696.1:p.Asp1811Ala
XM_017018372.2:c.5408A>C (SBF2)	XP_016873861.1:p.Asp1803Ala
XM_017018373.2:c.5408A>C (SBF2)	XP_016873862.1:p.Asp1803Ala
XM_017018374.2:c.5321A>C (SBF2)	XP_016873863.1:p.Asp1774Ala
XM_017018375.2:c.5309A>C (SBF2)	XP_016873864.1:p.Asp1770Ala
XR_001747994.2:n.5557A>C (SBF2)
XR_001748470.1:n.200+933T>G
XR_001748471.1:n.85+933T>G
NM_001386339.1:c.5546A>C (SBF2)	NP_001373268.1:p.Asp1849Ala
NM_001386342.1:c.5321A>C (SBF2)	NP_001373271.1:p.Asp1774Ala
NM_030962.4:c.5450A>C (SBF2) MANE Select	NP_112224.1:p.Asp1817Ala