Canonical Allele Identifier: CA1951790220

Gene: SBF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9832274T= , CM000673.2:g.9832274T=	GRCh38
NC_000011.9:g.9853821T= , CM000673.1:g.9853821T=	GRCh37
NC_000011.8:g.9810397T=	NCBI36
NG_008074.1:g.466934A= , LRG_267:g.466934A=

Transcript Alleles

HGVS	Amino-acid Change
NM_030962.4:c.3602A= MANE Select	NP_112224.1:p.His1201=
ENST00000256190.13:c.3602A= MANE Select	ENSP00000256190.8:p.His1201=
NM_001386339.1:c.3602A=	NP_001373268.1:p.His1201=
NM_001386342.1:c.3473A=	NP_001373271.1:p.His1158=
NM_030962.3:c.3602A= , LRG_267t1:c.3602A=	NP_112224.1:p.His1201=
ENST00000256190.12:c.3602A=	ENSP00000256190.8:p.His1201=
ENST00000530741.1:c.253A=
ENST00000530741.2:c.2306A=	ENSP00000432643.2:p.His769=
ENST00000617179.4:c.3461A=	ENSP00000482806.1:p.His1154=
ENST00000675281.1:c.3602A=	ENSP00000502491.1:p.His1201=
ENST00000675281.2:c.3602A=	ENSP00000502491.1:p.His1201=
ENST00000676324.1:c.3602A=	ENSP00000502578.1:p.His1201=
ENST00000676324.2:c.3602A=	ENSP00000502578.1:p.His1201=
ENST00000676387.1:c.3488A=	ENSP00000502779.1:p.His1163=
ENST00000676387.2:c.3488A=	ENSP00000502779.1:p.His1163=
ENST00000688344.1:c.3209A=	ENSP00000509987.1:p.His1070=
ENST00000689128.1:c.3602A=	ENSP00000509587.1:p.His1201=
ENST00000689258.1:c.3464A=	ENSP00000510475.1:p.His1155=
ENST00000689356.1:n.773A=
ENST00000689597.1:c.2306A=	ENSP00000510781.1:p.His769=
ENST00000689674.1:c.2496A=	ENSP00000510723.1:n.2496A=
ENST00000689940.1:c.3596A=	ENSP00000508452.1:p.His1199=
ENST00000690003.1:c.2401A=	ENSP00000508748.1:n.2401A=
ENST00000692716.1:c.3473A=	ENSP00000509545.1:p.His1158=
ENST00000693181.1:c.2431A=	ENSP00000510179.1:n.2431A=
XM_005253154.3:c.3602A=	XP_005253211.1:p.His1201=
XM_005253154.5:c.3602A=	XP_005253211.1:p.His1201=
XM_005253155.3:c.3473A=	XP_005253212.1:p.His1158=
XM_005253155.5:c.3473A=	XP_005253212.1:p.His1158=
XM_011520394.1:c.3488A=	XP_011518696.1:p.His1163=
XM_011520394.3:c.3488A=	XP_011518696.1:p.His1163=
XM_011520395.1:c.3602A=	XP_011518697.1:p.His1201=
XM_011520395.3:c.3602A=	XP_011518697.1:p.His1201=
XM_017018372.2:c.3464A=	XP_016873861.1:p.His1155=
XM_017018373.2:c.3464A=	XP_016873862.1:p.His1155=
XM_017018374.2:c.3473A=	XP_016873863.1:p.His1158=
XM_017018375.2:c.3602A=	XP_016873864.1:p.His1201=
XM_017018376.2:c.3602A=	XP_016873865.1:p.His1201=
XR_001747994.2:n.3740A=