Canonical Allele Identifier: CA473053739

Gene: SBF2 SBF2-AS1

Linked Data

• MyVariant Identifiers: chr11:g.9803060G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9781513G>A , CM000673.2:g.9781513G>A	GRCh38
NC_000011.9:g.9803060G>A , CM000673.1:g.9803060G>A	GRCh37
NC_000011.8:g.9759636G>A	NCBI36
NG_008074.1:g.517695C>T , LRG_267:g.517695C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524961.6:n.1929C>T (SBF2)
ENST00000675281.2:c.5520C>T (SBF2)	ENSP00000502491.1:p.Phe1840=
ENST00000676324.2:c.*1753C>T (SBF2)	ENSP00000502578.1:n.*1753C>T
ENST00000676387.2:c.5502C>T (SBF2)	ENSP00000502779.1:p.Phe1834=
ENST00000688344.1:c.5052C>T (SBF2)	ENSP00000509987.1:p.Phe1684=
ENST00000689128.1:c.5541C>T (SBF2)	ENSP00000509587.1:p.Phe1847=
ENST00000689258.1:c.5382C>T (SBF2)	ENSP00000510475.1:p.Phe1794=
ENST00000689342.1:c.1611C>T (SBF2)
ENST00000689356.1:n.2616C>T (SBF2)
ENST00000689940.1:c.5439C>T (SBF2)	ENSP00000508452.1:p.Phe1813=
ENST00000690437.1:n.1394C>T (SBF2)
ENST00000690944.1:c.1525C>T (SBF2)
ENST00000691616.1:n.1921C>T (SBF2)
ENST00000692716.1:c.5316C>T (SBF2)	ENSP00000509545.1:p.Phe1772=
ENST00000693541.1:n.2364C>T (SBF2)
ENST00000256190.13:c.5445C>T (SBF2) MANE Select	ENSP00000256190.8:p.Phe1815=
ENST00000675281.1:c.5520C>T (SBF2)	ENSP00000502491.1:p.Phe1840=
ENST00000676324.1:c.*1753C>T (SBF2)	ENSP00000502578.1:n.*1753C>T
ENST00000676387.1:c.5502C>T (SBF2)	ENSP00000502779.1:p.Phe1834=
ENST00000256190.12:c.5445C>T (SBF2)	ENSP00000256190.8:p.Phe1815=
ENST00000525040.5:n.748C>T (SBF2)
ENST00000617179.4:c.5304C>T (SBF2)	ENSP00000482806.1:p.Phe1768=
NM_030962.3:c.5445C>T , LRG_267t1:c.5445C>T (SBF2)	NP_112224.1:p.Phe1815=
NR_036485.1:n.211+23010G>A (SBF2-AS1)
XM_005253154.3:c.5541C>T (SBF2)	XP_005253211.1:p.Phe1847=
XM_005253155.3:c.5412C>T (SBF2)	XP_005253212.1:p.Phe1804=
XM_011520394.1:c.5427C>T (SBF2)	XP_011518696.1:p.Phe1809=
XR_931024.1:n.200+938G>A
XR_931025.1:n.200+938G>A
XM_005253154.5:c.5541C>T (SBF2)	XP_005253211.1:p.Phe1847=
XM_005253155.5:c.5412C>T (SBF2)	XP_005253212.1:p.Phe1804=
XM_011520394.3:c.5427C>T (SBF2)	XP_011518696.1:p.Phe1809=
XM_017018372.2:c.5403C>T (SBF2)	XP_016873861.1:p.Phe1801=
XM_017018373.2:c.5403C>T (SBF2)	XP_016873862.1:p.Phe1801=
XM_017018374.2:c.5316C>T (SBF2)	XP_016873863.1:p.Phe1772=
XM_017018375.2:c.5304C>T (SBF2)	XP_016873864.1:p.Phe1768=
XR_001747994.2:n.5552C>T (SBF2)
XR_001748470.1:n.200+938G>A
XR_001748471.1:n.85+938G>A
NM_001386339.1:c.5541C>T (SBF2)	NP_001373268.1:p.Phe1847=
NM_001386342.1:c.5316C>T (SBF2)	NP_001373271.1:p.Phe1772=
NM_030962.4:c.5445C>T (SBF2) MANE Select	NP_112224.1:p.Phe1815=