Canonical Allele Identifier: CA379629969

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9803056C>A (hg19) ; chr11:g.9781509C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781509C>A , CM000673.2:g.9781509C>A	GRCh38
NC_000011.9:g.9803056C>A , CM000673.1:g.9803056C>A	GRCh37
NC_000011.8:g.9759632C>A	NCBI36
NG_008074.1:g.517699G>T , LRG_267:g.517699G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1933G>T (SBF2)
ENST00000675281.2:c.5524G>T (SBF2)	ENSP00000502491.1:p.Asp1842Tyr
ENST00000676324.2:c.*1757G>T (SBF2)	ENSP00000502578.1:n.*1757G>T
ENST00000676387.2:c.5506G>T (SBF2)	ENSP00000502779.1:p.Asp1836Tyr
ENST00000688344.1:c.5056G>T (SBF2)	ENSP00000509987.1:p.Asp1686Tyr
ENST00000689128.1:c.5545G>T (SBF2)	ENSP00000509587.1:p.Asp1849Tyr
ENST00000689258.1:c.5386G>T (SBF2)	ENSP00000510475.1:p.Asp1796Tyr
ENST00000689342.1:c.1615G>T (SBF2)
ENST00000689356.1:n.2620G>T (SBF2)
ENST00000689940.1:c.5443G>T (SBF2)	ENSP00000508452.1:p.Asp1815Tyr
ENST00000690437.1:n.1398G>T (SBF2)
ENST00000690944.1:c.1529G>T (SBF2)
ENST00000691616.1:n.1925G>T (SBF2)
ENST00000692716.1:c.5320G>T (SBF2)	ENSP00000509545.1:p.Asp1774Tyr
ENST00000693541.1:n.2368G>T (SBF2)
ENST00000256190.13:c.5449G>T (SBF2) MANE Select	ENSP00000256190.8:p.Asp1817Tyr
ENST00000675281.1:c.5524G>T (SBF2)	ENSP00000502491.1:p.Asp1842Tyr
ENST00000676324.1:c.*1757G>T (SBF2)	ENSP00000502578.1:n.*1757G>T
ENST00000676387.1:c.5506G>T (SBF2)	ENSP00000502779.1:p.Asp1836Tyr
ENST00000256190.12:c.5449G>T (SBF2)	ENSP00000256190.8:p.Asp1817Tyr
ENST00000525040.5:n.752G>T (SBF2)
ENST00000617179.4:c.5308G>T (SBF2)	ENSP00000482806.1:p.Asp1770Tyr
NM_030962.3:c.5449G>T , LRG_267t1:c.5449G>T (SBF2)	NP_112224.1:p.Asp1817Tyr
NR_036485.1:n.211+23006C>A (SBF2-AS1)
XM_005253154.3:c.5545G>T (SBF2)	XP_005253211.1:p.Asp1849Tyr
XM_005253155.3:c.5416G>T (SBF2)	XP_005253212.1:p.Asp1806Tyr
XM_011520394.1:c.5431G>T (SBF2)	XP_011518696.1:p.Asp1811Tyr
XR_931024.1:n.200+934C>A
XR_931025.1:n.200+934C>A
XM_005253154.5:c.5545G>T (SBF2)	XP_005253211.1:p.Asp1849Tyr
XM_005253155.5:c.5416G>T (SBF2)	XP_005253212.1:p.Asp1806Tyr
XM_011520394.3:c.5431G>T (SBF2)	XP_011518696.1:p.Asp1811Tyr
XM_017018372.2:c.5407G>T (SBF2)	XP_016873861.1:p.Asp1803Tyr
XM_017018373.2:c.5407G>T (SBF2)	XP_016873862.1:p.Asp1803Tyr
XM_017018374.2:c.5320G>T (SBF2)	XP_016873863.1:p.Asp1774Tyr
XM_017018375.2:c.5308G>T (SBF2)	XP_016873864.1:p.Asp1770Tyr
XR_001747994.2:n.5556G>T (SBF2)
XR_001748470.1:n.200+934C>A
XR_001748471.1:n.85+934C>A
NM_001386339.1:c.5545G>T (SBF2)	NP_001373268.1:p.Asp1849Tyr
NM_001386342.1:c.5320G>T (SBF2)	NP_001373271.1:p.Asp1774Tyr
NM_030962.4:c.5449G>T (SBF2) MANE Select	NP_112224.1:p.Asp1817Tyr