Canonical Allele Identifier: CA670793861

Gene: SBF2

Linked Data

• dbSNP Id: rs1284393246
• MyVariant Identifiers: chr11:g.10228578C>A (hg19) ; chr11:g.10207031C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.10207031C>A , CM000673.2:g.10207031C>A	GRCh38
NC_000011.9:g.10228578C>A , CM000673.1:g.10228578C>A	GRCh37
NC_000011.8:g.10185154C>A	NCBI36
NG_008074.1:g.92177G>T , LRG_267:g.92177G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526353.2:n.206-13044G>T
ENST00000533770.6:c.56-13044G>T	ENSP00000509247.1:n.56-13044G>T
ENST00000675281.2:c.56-13044G>T	ENSP00000502491.1:n.56-13044G>T
ENST00000676324.2:c.56-13044G>T	ENSP00000502578.1:n.56-13044G>T
ENST00000676387.2:c.56-13044G>T	ENSP00000502779.1:n.56-13044G>T
ENST00000685217.1:n.387-13044G>T
ENST00000686079.1:c.56-13044G>T	ENSP00000509599.1:n.56-13044G>T
ENST00000686677.1:n.194-13044G>T
ENST00000687210.1:c.56-13044G>T	ENSP00000509480.1:n.56-13044G>T
ENST00000687256.1:c.56-13044G>T	ENSP00000508741.1:n.56-13044G>T
ENST00000687300.1:c.56-13044G>T	ENSP00000508415.1:n.56-13044G>T
ENST00000688206.1:c.56-13044G>T	ENSP00000510516.1:n.56-13044G>T
ENST00000688417.1:n.206-13044G>T
ENST00000688739.1:c.55+86984G>T	ENSP00000510449.1:n.55+86984G>T
ENST00000689128.1:c.56-13044G>T	ENSP00000509587.1:n.56-13044G>T
ENST00000689258.1:c.56-13044G>T	ENSP00000510475.1:n.56-13044G>T
ENST00000689940.1:c.56-13044G>T	ENSP00000508452.1:n.56-13044G>T
ENST00000690806.1:c.56-13044G>T	ENSP00000509417.1:n.56-13044G>T
ENST00000690959.1:n.196-13044G>T
ENST00000692068.1:c.56-13044G>T	ENSP00000510763.1:n.56-13044G>T
ENST00000692716.1:c.56-13044G>T	ENSP00000509545.1:n.56-13044G>T
ENST00000693022.1:c.56-13044G>T	ENSP00000508914.1:n.56-13044G>T
ENST00000693201.1:c.56-13044G>T	ENSP00000510346.1:n.56-13044G>T
ENST00000693212.1:c.56-13044G>T	ENSP00000510716.1:n.56-13044G>T
ENST00000256190.13:c.56-13044G>T MANE Select	ENSP00000256190.8:n.56-13044G>T
ENST00000675281.1:c.56-13044G>T	ENSP00000502491.1:n.56-13044G>T
ENST00000676324.1:c.56-13044G>T	ENSP00000502578.1:n.56-13044G>T
ENST00000676387.1:c.56-13044G>T	ENSP00000502779.1:n.56-13044G>T
ENST00000256190.12:c.56-13044G>T	ENSP00000256190.8:n.56-13044G>T
NM_030962.3:c.56-13044G>T , LRG_267t1:c.56-13044G>T	NP_112224.1:n.56-13044G>T
XM_005253154.3:c.56-13044G>T	XP_005253211.1:n.56-13044G>T
XM_005253155.3:c.56-13044G>T	XP_005253212.1:n.56-13044G>T
XM_011520394.1:c.56-13044G>T	XP_011518696.1:n.56-13044G>T
XM_011520395.1:c.56-13044G>T	XP_011518697.1:n.56-13044G>T
XM_011520396.1:c.56-13044G>T	XP_011518698.1:n.56-13044G>T
XM_005253154.5:c.56-13044G>T	XP_005253211.1:n.56-13044G>T
XM_005253155.5:c.56-13044G>T	XP_005253212.1:n.56-13044G>T
XM_011520394.3:c.56-13044G>T	XP_011518696.1:n.56-13044G>T
XM_011520395.3:c.56-13044G>T	XP_011518697.1:n.56-13044G>T
XM_011520396.3:c.56-13044G>T	XP_011518698.1:n.56-13044G>T
XM_017018374.2:c.56-13044G>T	XP_016873863.1:n.56-13044G>T
XM_017018375.2:c.56-13044G>T	XP_016873864.1:n.56-13044G>T
XM_017018376.2:c.56-13044G>T	XP_016873865.1:n.56-13044G>T
XM_017018377.2:c.56-13044G>T	XP_016873866.1:n.56-13044G>T
XR_001747994.2:n.194-13044G>T
NM_001386339.1:c.56-13044G>T	NP_001373268.1:n.56-13044G>T
NM_001386342.1:c.56-13044G>T	NP_001373271.1:n.56-13044G>T
NM_030962.4:c.56-13044G>T MANE Select	NP_112224.1:n.56-13044G>T