Canonical Allele Identifier: CA10577431
Gene: SBF2 HGNC NCBI
SBF2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9808900C>T , CM000673.2:g.9808900C>T GRCh38
NC_000011.9:g.9830447C>T , CM000673.1:g.9830447C>T GRCh37
NC_000011.8:g.9787023C>T NCBI36
NG_008074.1:g.490308G>A , LRG_267:g.490308G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000524961.6:n.741+1G>A (SBF2)
ENST00000530741.2:c.2820+1G>A (SBF2) ENSP00000432643.2:n.2820+1G>A
ENST00000532095.2:n.793+1G>A (SBF2)
ENST00000675281.2:c.4332+1G>A (SBF2) ENSP00000502491.1:n.4332+1G>A
ENST00000676324.2:c.*565+1G>A (SBF2) ENSP00000502578.1:n.*565+1G>A
ENST00000676387.2:c.4314+1G>A (SBF2) ENSP00000502779.1:n.4314+1G>A
ENST00000688344.1:c.3864+1G>A (SBF2) ENSP00000509987.1:n.3864+1G>A
ENST00000689128.1:c.4353+1G>A (SBF2) ENSP00000509587.1:n.4353+1G>A
ENST00000689258.1:c.4194+1G>A (SBF2) ENSP00000510475.1:n.4194+1G>A
ENST00000689342.1:c.464+1G>A (SBF2)
ENST00000689356.1:n.1428+1G>A (SBF2)
ENST00000689597.1:c.2961+1G>A (SBF2) ENSP00000510781.1:n.2961+1G>A
ENST00000689940.1:c.4251+1G>A (SBF2) ENSP00000508452.1:n.4251+1G>A
ENST00000690944.1:c.464+1G>A (SBF2)
ENST00000691616.1:n.733+1G>A (SBF2)
ENST00000692716.1:c.4128+1G>A (SBF2) ENSP00000509545.1:n.4128+1G>A
ENST00000693541.1:n.1176+1G>A (SBF2)
ENST00000256190.13:c.4257+1G>A (SBF2) MANE Select ENSP00000256190.8:n.4257+1G>A
ENST00000675281.1:c.4332+1G>A (SBF2) ENSP00000502491.1:n.4332+1G>A
ENST00000676324.1:c.*565+1G>A (SBF2) ENSP00000502578.1:n.*565+1G>A
ENST00000676387.1:c.4314+1G>A (SBF2) ENSP00000502779.1:n.4314+1G>A
ENST00000256190.12:c.4257+1G>A (SBF2) ENSP00000256190.8:n.4257+1G>A
ENST00000525697.1:n.597G>A (SBF2)
ENST00000528478.1:n.325+1G>A (SBF2)
ENST00000617179.4:c.4116+1G>A (SBF2) ENSP00000482806.1:n.4116+1G>A
NM_030962.3:c.4257+1G>A , LRG_267t1:c.4257+1G>A (SBF2) NP_112224.1:n.4257+1G>A
NR_036485.1:n.1264C>T (SBF2-AS1)
XM_005253154.3:c.4353+1G>A (SBF2) XP_005253211.1:n.4353+1G>A
XM_005253155.3:c.4224+1G>A (SBF2) XP_005253212.1:n.4224+1G>A
XM_011520394.1:c.4239+1G>A (SBF2) XP_011518696.1:n.4239+1G>A
XM_005253154.5:c.4353+1G>A (SBF2) XP_005253211.1:n.4353+1G>A
XM_005253155.5:c.4224+1G>A (SBF2) XP_005253212.1:n.4224+1G>A
XM_011520394.3:c.4239+1G>A (SBF2) XP_011518696.1:n.4239+1G>A
XM_017018372.2:c.4215+1G>A (SBF2) XP_016873861.1:n.4215+1G>A
XM_017018373.2:c.4215+1G>A (SBF2) XP_016873862.1:n.4215+1G>A
XM_017018374.2:c.4128+1G>A (SBF2) XP_016873863.1:n.4128+1G>A
XM_017018375.2:c.4116+1G>A (SBF2) XP_016873864.1:n.4116+1G>A
XR_001747994.2:n.4491+1G>A (SBF2)
NM_001386339.1:c.4353+1G>A (SBF2) NP_001373268.1:n.4353+1G>A
NM_001386342.1:c.4128+1G>A (SBF2) NP_001373271.1:n.4128+1G>A
NM_030962.4:c.4257+1G>A (SBF2) MANE Select NP_112224.1:n.4257+1G>A