Canonical Allele Identifier: CA379645482

Gene: SBF2

Linked Data

• MyVariant Identifiers: chr11:g.9853785T>G (hg19) ; chr11:g.9832238T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9832238T>G , CM000673.2:g.9832238T>G	GRCh38
NC_000011.9:g.9853785T>G , CM000673.1:g.9853785T>G	GRCh37
NC_000011.8:g.9810361T>G	NCBI36
NG_008074.1:g.466970A>C , LRG_267:g.466970A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000530741.2:c.2342A>C	ENSP00000432643.2:p.Asn781Thr
ENST00000675281.2:c.3638A>C	ENSP00000502491.1:p.Asn1213Thr
ENST00000676324.2:c.3638A>C	ENSP00000502578.1:p.Asn1213Thr
ENST00000676387.2:c.3524A>C	ENSP00000502779.1:p.Asn1175Thr
ENST00000688344.1:c.3245A>C	ENSP00000509987.1:p.Asn1082Thr
ENST00000689128.1:c.3638A>C	ENSP00000509587.1:p.Asn1213Thr
ENST00000689258.1:c.3500A>C	ENSP00000510475.1:p.Asn1167Thr
ENST00000689356.1:n.809A>C
ENST00000689597.1:c.2342A>C	ENSP00000510781.1:p.Asn781Thr
ENST00000689674.1:c.2532A>C	ENSP00000510723.1:n.2532A>C
ENST00000689940.1:c.3632A>C	ENSP00000508452.1:p.Asn1211Thr
ENST00000690003.1:c.2437A>C	ENSP00000508748.1:n.2437A>C
ENST00000692716.1:c.3509A>C	ENSP00000509545.1:p.Asn1170Thr
ENST00000693181.1:c.2467A>C	ENSP00000510179.1:n.2467A>C
ENST00000256190.13:c.3638A>C MANE Select	ENSP00000256190.8:p.Asn1213Thr
ENST00000675281.1:c.3638A>C	ENSP00000502491.1:p.Asn1213Thr
ENST00000676324.1:c.3638A>C	ENSP00000502578.1:p.Asn1213Thr
ENST00000676387.1:c.3524A>C	ENSP00000502779.1:p.Asn1175Thr
ENST00000256190.12:c.3638A>C	ENSP00000256190.8:p.Asn1213Thr
ENST00000530741.1:c.289A>C
ENST00000617179.4:c.3497A>C	ENSP00000482806.1:p.Asn1166Thr
NM_030962.3:c.3638A>C , LRG_267t1:c.3638A>C	NP_112224.1:p.Asn1213Thr
XM_005253154.3:c.3638A>C	XP_005253211.1:p.Asn1213Thr
XM_005253155.3:c.3509A>C	XP_005253212.1:p.Asn1170Thr
XM_011520394.1:c.3524A>C	XP_011518696.1:p.Asn1175Thr
XM_011520395.1:c.3638A>C	XP_011518697.1:p.Asn1213Thr
XM_005253154.5:c.3638A>C	XP_005253211.1:p.Asn1213Thr
XM_005253155.5:c.3509A>C	XP_005253212.1:p.Asn1170Thr
XM_011520394.3:c.3524A>C	XP_011518696.1:p.Asn1175Thr
XM_011520395.3:c.3638A>C	XP_011518697.1:p.Asn1213Thr
XM_017018372.2:c.3500A>C	XP_016873861.1:p.Asn1167Thr
XM_017018373.2:c.3500A>C	XP_016873862.1:p.Asn1167Thr
XM_017018374.2:c.3509A>C	XP_016873863.1:p.Asn1170Thr
XM_017018375.2:c.3638A>C	XP_016873864.1:p.Asn1213Thr
XM_017018376.2:c.3638A>C	XP_016873865.1:p.Asn1213Thr
XR_001747994.2:n.3776A>C
NM_001386339.1:c.3638A>C	NP_001373268.1:p.Asn1213Thr
NM_001386342.1:c.3509A>C	NP_001373271.1:p.Asn1170Thr
NM_030962.4:c.3638A>C MANE Select	NP_112224.1:p.Asn1213Thr