Canonical Allele Identifier: CA379629974
Gene: SBF2 HGNC NCBI
SBF2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9781510A>C , CM000673.2:g.9781510A>C GRCh38
NC_000011.9:g.9803057A>C , CM000673.1:g.9803057A>C GRCh37
NC_000011.8:g.9759633A>C NCBI36
NG_008074.1:g.517698T>G , LRG_267:g.517698T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000524961.6:n.1932T>G (SBF2)
ENST00000675281.2:c.5523T>G (SBF2) ENSP00000502491.1:p.Phe1841Leu
ENST00000676324.2:c.*1756T>G (SBF2) ENSP00000502578.1:n.*1756T>G
ENST00000676387.2:c.5505T>G (SBF2) ENSP00000502779.1:p.Phe1835Leu
ENST00000688344.1:c.5055T>G (SBF2) ENSP00000509987.1:p.Phe1685Leu
ENST00000689128.1:c.5544T>G (SBF2) ENSP00000509587.1:p.Phe1848Leu
ENST00000689258.1:c.5385T>G (SBF2) ENSP00000510475.1:p.Phe1795Leu
ENST00000689342.1:c.1614T>G (SBF2)
ENST00000689356.1:n.2619T>G (SBF2)
ENST00000689940.1:c.5442T>G (SBF2) ENSP00000508452.1:p.Phe1814Leu
ENST00000690437.1:n.1397T>G (SBF2)
ENST00000690944.1:c.1528T>G (SBF2)
ENST00000691616.1:n.1924T>G (SBF2)
ENST00000692716.1:c.5319T>G (SBF2) ENSP00000509545.1:p.Phe1773Leu
ENST00000693541.1:n.2367T>G (SBF2)
ENST00000256190.13:c.5448T>G (SBF2) MANE Select ENSP00000256190.8:p.Phe1816Leu
ENST00000675281.1:c.5523T>G (SBF2) ENSP00000502491.1:p.Phe1841Leu
ENST00000676324.1:c.*1756T>G (SBF2) ENSP00000502578.1:n.*1756T>G
ENST00000676387.1:c.5505T>G (SBF2) ENSP00000502779.1:p.Phe1835Leu
ENST00000256190.12:c.5448T>G (SBF2) ENSP00000256190.8:p.Phe1816Leu
ENST00000525040.5:n.751T>G (SBF2)
ENST00000617179.4:c.5307T>G (SBF2) ENSP00000482806.1:p.Phe1769Leu
NM_030962.3:c.5448T>G , LRG_267t1:c.5448T>G (SBF2) NP_112224.1:p.Phe1816Leu
NR_036485.1:n.211+23007A>C (SBF2-AS1)
XM_005253154.3:c.5544T>G (SBF2) XP_005253211.1:p.Phe1848Leu
XM_005253155.3:c.5415T>G (SBF2) XP_005253212.1:p.Phe1805Leu
XM_011520394.1:c.5430T>G (SBF2) XP_011518696.1:p.Phe1810Leu
XR_931024.1:n.200+935A>C
XR_931025.1:n.200+935A>C
XM_005253154.5:c.5544T>G (SBF2) XP_005253211.1:p.Phe1848Leu
XM_005253155.5:c.5415T>G (SBF2) XP_005253212.1:p.Phe1805Leu
XM_011520394.3:c.5430T>G (SBF2) XP_011518696.1:p.Phe1810Leu
XM_017018372.2:c.5406T>G (SBF2) XP_016873861.1:p.Phe1802Leu
XM_017018373.2:c.5406T>G (SBF2) XP_016873862.1:p.Phe1802Leu
XM_017018374.2:c.5319T>G (SBF2) XP_016873863.1:p.Phe1773Leu
XM_017018375.2:c.5307T>G (SBF2) XP_016873864.1:p.Phe1769Leu
XR_001747994.2:n.5555T>G (SBF2)
XR_001748470.1:n.200+935A>C
XR_001748471.1:n.85+935A>C
NM_001386339.1:c.5544T>G (SBF2) NP_001373268.1:p.Phe1848Leu
NM_001386342.1:c.5319T>G (SBF2) NP_001373271.1:p.Phe1773Leu
NM_030962.4:c.5448T>G (SBF2) MANE Select NP_112224.1:p.Phe1816Leu