Canonical Allele Identifier: CA935022904

Gene: SBF2 SBF2-AS1

Linked Data

• dbSNP Id: rs1851984409
• gnomAD v3: 11-9781224-A-AAATAACTAACAAC
• gnomAD v4: 11-9781224-A-AAATAACTAACAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781226_9781238dup , CM000673.2:g.9781226_9781238dup	GRCh38
NC_000011.9:g.9802773_9802785dup , CM000673.1:g.9802773_9802785dup	GRCh37
NC_000011.8:g.9759349_9759361dup	NCBI36
NG_008074.1:g.517971_517983dup , LRG_267:g.517971_517983dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1935+270_1935+282dup (SBF2)
ENST00000675281.2:c.5526+270_5526+282dup (SBF2)	ENSP00000502491.1:n.5526+270_5526+282dup
ENST00000676324.2:c.*1759+270_*1759+282dup (SBF2)	ENSP00000502578.1:n.*1759+270_*1759+282dup
ENST00000676387.2:c.5508+270_5508+282dup (SBF2)	ENSP00000502779.1:n.5508+270_5508+282dup
ENST00000688344.1:c.5058+270_5058+282dup (SBF2)	ENSP00000509987.1:n.5058+270_5058+282dup
ENST00000689128.1:c.5547+270_5547+282dup (SBF2)	ENSP00000509587.1:n.5547+270_5547+282dup
ENST00000689258.1:c.5388+270_5388+282dup (SBF2)	ENSP00000510475.1:n.5388+270_5388+282dup
ENST00000689342.1:c.1617+270_1617+282dup (SBF2)
ENST00000689356.1:n.2622+270_2622+282dup (SBF2)
ENST00000689940.1:c.5445+270_5445+282dup (SBF2)	ENSP00000508452.1:n.5445+270_5445+282dup
ENST00000690437.1:n.1400+270_1400+282dup (SBF2)
ENST00000690944.1:c.1531+270_1531+282dup (SBF2)
ENST00000691616.1:n.1927+270_1927+282dup (SBF2)
ENST00000692716.1:c.5322+270_5322+282dup (SBF2)	ENSP00000509545.1:n.5322+270_5322+282dup
ENST00000693541.1:n.2370+270_2370+282dup (SBF2)
ENST00000256190.13:c.5451+270_5451+282dup (SBF2) MANE Select	ENSP00000256190.8:n.5451+270_5451+282dup
ENST00000675281.1:c.5526+270_5526+282dup (SBF2)	ENSP00000502491.1:n.5526+270_5526+282dup
ENST00000676324.1:c.*1759+270_*1759+282dup (SBF2)	ENSP00000502578.1:n.*1759+270_*1759+282dup
ENST00000676387.1:c.5508+270_5508+282dup (SBF2)	ENSP00000502779.1:n.5508+270_5508+282dup
ENST00000256190.12:c.5451+270_5451+282dup (SBF2)	ENSP00000256190.8:n.5451+270_5451+282dup
ENST00000525040.5:n.754+270_754+282dup (SBF2)
ENST00000617179.4:c.5310+270_5310+282dup (SBF2)	ENSP00000482806.1:n.5310+270_5310+282dup
NM_030962.3:c.5451+270_5451+282dup , LRG_267t1:c.5451+270_5451+282dup (SBF2)	NP_112224.1:n.5451+270_5451+282dup
NR_036485.1:n.211+22723_211+22735dup (SBF2-AS1)
XM_005253154.3:c.5547+270_5547+282dup (SBF2)	XP_005253211.1:n.5547+270_5547+282dup
XM_005253155.3:c.5418+270_5418+282dup (SBF2)	XP_005253212.1:n.5418+270_5418+282dup
XM_011520394.1:c.5433+270_5433+282dup (SBF2)	XP_011518696.1:n.5433+270_5433+282dup
XR_931024.1:n.200+651_200+663dup
XR_931025.1:n.200+651_200+663dup
XM_005253154.5:c.5547+270_5547+282dup (SBF2)	XP_005253211.1:n.5547+270_5547+282dup
XM_005253155.5:c.5418+270_5418+282dup (SBF2)	XP_005253212.1:n.5418+270_5418+282dup
XM_011520394.3:c.5433+270_5433+282dup (SBF2)	XP_011518696.1:n.5433+270_5433+282dup
XM_017018372.2:c.5409+270_5409+282dup (SBF2)	XP_016873861.1:n.5409+270_5409+282dup
XM_017018373.2:c.5409+270_5409+282dup (SBF2)	XP_016873862.1:n.5409+270_5409+282dup
XM_017018374.2:c.5322+270_5322+282dup (SBF2)	XP_016873863.1:n.5322+270_5322+282dup
XM_017018375.2:c.5310+270_5310+282dup (SBF2)	XP_016873864.1:n.5310+270_5310+282dup
XR_001747994.2:n.5558+270_5558+282dup (SBF2)
XR_001748470.1:n.200+651_200+663dup
XR_001748471.1:n.85+651_85+663dup
NM_001386339.1:c.5547+270_5547+282dup (SBF2)	NP_001373268.1:n.5547+270_5547+282dup
NM_001386342.1:c.5322+270_5322+282dup (SBF2)	NP_001373271.1:n.5322+270_5322+282dup
NM_030962.4:c.5451+270_5451+282dup (SBF2) MANE Select	NP_112224.1:n.5451+270_5451+282dup