Canonical Allele Identifier: CA379634296
Gene: SBF2 HGNC NCBI
SBF2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9789282T>A , CM000673.2:g.9789282T>A GRCh38
NC_000011.9:g.9810829T>A , CM000673.1:g.9810829T>A GRCh37
NC_000011.8:g.9767405T>A NCBI36
NG_008074.1:g.509926A>T , LRG_267:g.509926A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000524961.6:n.1243A>T (SBF2)
ENST00000532095.2:n.1295A>T (SBF2)
ENST00000675281.2:c.4834A>T (SBF2) ENSP00000502491.1:p.Thr1612Ser
ENST00000676324.2:c.*1067A>T (SBF2) ENSP00000502578.1:n.*1067A>T
ENST00000676387.2:c.4816A>T (SBF2) ENSP00000502779.1:p.Thr1606Ser
ENST00000688344.1:c.4366A>T (SBF2) ENSP00000509987.1:p.Thr1456Ser
ENST00000689128.1:c.4855A>T (SBF2) ENSP00000509587.1:p.Thr1619Ser
ENST00000689258.1:c.4696A>T (SBF2) ENSP00000510475.1:p.Thr1566Ser
ENST00000689342.1:c.925A>T (SBF2)
ENST00000689356.1:n.1930A>T (SBF2)
ENST00000689597.1:c.3463A>T (SBF2) ENSP00000510781.1:p.Thr1155Ser
ENST00000689940.1:c.4753A>T (SBF2) ENSP00000508452.1:p.Thr1585Ser
ENST00000690944.1:c.839A>T (SBF2)
ENST00000691616.1:n.1235A>T (SBF2)
ENST00000692716.1:c.4630A>T (SBF2) ENSP00000509545.1:p.Thr1544Ser
ENST00000693541.1:n.1678A>T (SBF2)
ENST00000256190.13:c.4759A>T (SBF2) MANE Select ENSP00000256190.8:p.Thr1587Ser
ENST00000675281.1:c.4834A>T (SBF2) ENSP00000502491.1:p.Thr1612Ser
ENST00000676324.1:c.*1067A>T (SBF2) ENSP00000502578.1:n.*1067A>T
ENST00000676387.1:c.4816A>T (SBF2) ENSP00000502779.1:p.Thr1606Ser
ENST00000256190.12:c.4759A>T (SBF2) ENSP00000256190.8:p.Thr1587Ser
ENST00000617179.4:c.4618A>T (SBF2) ENSP00000482806.1:p.Thr1540Ser
NM_030962.3:c.4759A>T , LRG_267t1:c.4759A>T (SBF2) NP_112224.1:p.Thr1587Ser
NR_036485.1:n.212-18566T>A (SBF2-AS1)
XM_005253154.3:c.4855A>T (SBF2) XP_005253211.1:p.Thr1619Ser
XM_005253155.3:c.4726A>T (SBF2) XP_005253212.1:p.Thr1576Ser
XM_011520394.1:c.4741A>T (SBF2) XP_011518696.1:p.Thr1581Ser
XR_931024.1:n.456-1587T>A
XR_931025.1:n.271-1587T>A
XM_005253154.5:c.4855A>T (SBF2) XP_005253211.1:p.Thr1619Ser
XM_005253155.5:c.4726A>T (SBF2) XP_005253212.1:p.Thr1576Ser
XM_011520394.3:c.4741A>T (SBF2) XP_011518696.1:p.Thr1581Ser
XM_017018372.2:c.4717A>T (SBF2) XP_016873861.1:p.Thr1573Ser
XM_017018373.2:c.4717A>T (SBF2) XP_016873862.1:p.Thr1573Ser
XM_017018374.2:c.4630A>T (SBF2) XP_016873863.1:p.Thr1544Ser
XM_017018375.2:c.4618A>T (SBF2) XP_016873864.1:p.Thr1540Ser
XR_001747994.2:n.4866A>T (SBF2)
NM_001386339.1:c.4855A>T (SBF2) NP_001373268.1:p.Thr1619Ser
NM_001386342.1:c.4630A>T (SBF2) NP_001373271.1:p.Thr1544Ser
NM_030962.4:c.4759A>T (SBF2) MANE Select NP_112224.1:p.Thr1587Ser