Canonical Allele Identifier: CA473070476

Gene: SBF2

Linked Data

• MyVariant Identifiers: chr11:g.9853790A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9832243A>C , CM000673.2:g.9832243A>C	GRCh38
NC_000011.9:g.9853790A>C , CM000673.1:g.9853790A>C	GRCh37
NC_000011.8:g.9810366A>C	NCBI36
NG_008074.1:g.466965T>G , LRG_267:g.466965T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000530741.2:c.2337T>G	ENSP00000432643.2:p.Ser779=
ENST00000675281.2:c.3633T>G	ENSP00000502491.1:p.Ser1211=
ENST00000676324.2:c.3633T>G	ENSP00000502578.1:p.Ser1211=
ENST00000676387.2:c.3519T>G	ENSP00000502779.1:p.Ser1173=
ENST00000688344.1:c.3240T>G	ENSP00000509987.1:p.Ser1080=
ENST00000689128.1:c.3633T>G	ENSP00000509587.1:p.Ser1211=
ENST00000689258.1:c.3495T>G	ENSP00000510475.1:p.Ser1165=
ENST00000689356.1:n.804T>G
ENST00000689597.1:c.2337T>G	ENSP00000510781.1:p.Ser779=
ENST00000689674.1:c.2527T>G	ENSP00000510723.1:n.2527T>G
ENST00000689940.1:c.3627T>G	ENSP00000508452.1:p.Ser1209=
ENST00000690003.1:c.2432T>G	ENSP00000508748.1:n.2432T>G
ENST00000692716.1:c.3504T>G	ENSP00000509545.1:p.Ser1168=
ENST00000693181.1:c.2462T>G	ENSP00000510179.1:n.2462T>G
ENST00000256190.13:c.3633T>G MANE Select	ENSP00000256190.8:p.Ser1211=
ENST00000675281.1:c.3633T>G	ENSP00000502491.1:p.Ser1211=
ENST00000676324.1:c.3633T>G	ENSP00000502578.1:p.Ser1211=
ENST00000676387.1:c.3519T>G	ENSP00000502779.1:p.Ser1173=
ENST00000256190.12:c.3633T>G	ENSP00000256190.8:p.Ser1211=
ENST00000530741.1:c.284T>G
ENST00000617179.4:c.3492T>G	ENSP00000482806.1:p.Ser1164=
NM_030962.3:c.3633T>G , LRG_267t1:c.3633T>G	NP_112224.1:p.Ser1211=
XM_005253154.3:c.3633T>G	XP_005253211.1:p.Ser1211=
XM_005253155.3:c.3504T>G	XP_005253212.1:p.Ser1168=
XM_011520394.1:c.3519T>G	XP_011518696.1:p.Ser1173=
XM_011520395.1:c.3633T>G	XP_011518697.1:p.Ser1211=
XM_005253154.5:c.3633T>G	XP_005253211.1:p.Ser1211=
XM_005253155.5:c.3504T>G	XP_005253212.1:p.Ser1168=
XM_011520394.3:c.3519T>G	XP_011518696.1:p.Ser1173=
XM_011520395.3:c.3633T>G	XP_011518697.1:p.Ser1211=
XM_017018372.2:c.3495T>G	XP_016873861.1:p.Ser1165=
XM_017018373.2:c.3495T>G	XP_016873862.1:p.Ser1165=
XM_017018374.2:c.3504T>G	XP_016873863.1:p.Ser1168=
XM_017018375.2:c.3633T>G	XP_016873864.1:p.Ser1211=
XM_017018376.2:c.3633T>G	XP_016873865.1:p.Ser1211=
XR_001747994.2:n.3771T>G
NM_001386339.1:c.3633T>G	NP_001373268.1:p.Ser1211=
NM_001386342.1:c.3504T>G	NP_001373271.1:p.Ser1168=
NM_030962.4:c.3633T>G MANE Select	NP_112224.1:p.Ser1211=