Canonical Allele Identifier: CA379645512

Gene: SBF2

Linked Data

• MyVariant Identifiers: chr11:g.9853798A>G (hg19) ; chr11:g.9832251A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9832251A>G , CM000673.2:g.9832251A>G	GRCh38
NC_000011.9:g.9853798A>G , CM000673.1:g.9853798A>G	GRCh37
NC_000011.8:g.9810374A>G	NCBI36
NG_008074.1:g.466957T>C , LRG_267:g.466957T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530741.2:c.2329T>C	ENSP00000432643.2:p.Phe777Leu
ENST00000675281.2:c.3625T>C	ENSP00000502491.1:p.Phe1209Leu
ENST00000676324.2:c.3625T>C	ENSP00000502578.1:p.Phe1209Leu
ENST00000676387.2:c.3511T>C	ENSP00000502779.1:p.Phe1171Leu
ENST00000688344.1:c.3232T>C	ENSP00000509987.1:p.Phe1078Leu
ENST00000689128.1:c.3625T>C	ENSP00000509587.1:p.Phe1209Leu
ENST00000689258.1:c.3487T>C	ENSP00000510475.1:p.Phe1163Leu
ENST00000689356.1:n.796T>C
ENST00000689597.1:c.2329T>C	ENSP00000510781.1:p.Phe777Leu
ENST00000689674.1:c.2519T>C	ENSP00000510723.1:n.2519T>C
ENST00000689940.1:c.3619T>C	ENSP00000508452.1:p.Phe1207Leu
ENST00000690003.1:c.2424T>C	ENSP00000508748.1:n.2424T>C
ENST00000692716.1:c.3496T>C	ENSP00000509545.1:p.Phe1166Leu
ENST00000693181.1:c.2454T>C	ENSP00000510179.1:n.2454T>C
ENST00000256190.13:c.3625T>C MANE Select	ENSP00000256190.8:p.Phe1209Leu
ENST00000675281.1:c.3625T>C	ENSP00000502491.1:p.Phe1209Leu
ENST00000676324.1:c.3625T>C	ENSP00000502578.1:p.Phe1209Leu
ENST00000676387.1:c.3511T>C	ENSP00000502779.1:p.Phe1171Leu
ENST00000256190.12:c.3625T>C	ENSP00000256190.8:p.Phe1209Leu
ENST00000530741.1:c.276T>C
ENST00000617179.4:c.3484T>C	ENSP00000482806.1:p.Phe1162Leu
NM_030962.3:c.3625T>C , LRG_267t1:c.3625T>C	NP_112224.1:p.Phe1209Leu
XM_005253154.3:c.3625T>C	XP_005253211.1:p.Phe1209Leu
XM_005253155.3:c.3496T>C	XP_005253212.1:p.Phe1166Leu
XM_011520394.1:c.3511T>C	XP_011518696.1:p.Phe1171Leu
XM_011520395.1:c.3625T>C	XP_011518697.1:p.Phe1209Leu
XM_005253154.5:c.3625T>C	XP_005253211.1:p.Phe1209Leu
XM_005253155.5:c.3496T>C	XP_005253212.1:p.Phe1166Leu
XM_011520394.3:c.3511T>C	XP_011518696.1:p.Phe1171Leu
XM_011520395.3:c.3625T>C	XP_011518697.1:p.Phe1209Leu
XM_017018372.2:c.3487T>C	XP_016873861.1:p.Phe1163Leu
XM_017018373.2:c.3487T>C	XP_016873862.1:p.Phe1163Leu
XM_017018374.2:c.3496T>C	XP_016873863.1:p.Phe1166Leu
XM_017018375.2:c.3625T>C	XP_016873864.1:p.Phe1209Leu
XM_017018376.2:c.3625T>C	XP_016873865.1:p.Phe1209Leu
XR_001747994.2:n.3763T>C
NM_001386339.1:c.3625T>C	NP_001373268.1:p.Phe1209Leu
NM_001386342.1:c.3496T>C	NP_001373271.1:p.Phe1166Leu
NM_030962.4:c.3625T>C MANE Select	NP_112224.1:p.Phe1209Leu