Canonical Allele Identifier: CA379630220
Gene: SBF2 HGNC NCBI
SBF2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9781553G>A , CM000673.2:g.9781553G>A GRCh38
NC_000011.9:g.9803100G>A , CM000673.1:g.9803100G>A GRCh37
NC_000011.8:g.9759676G>A NCBI36
NG_008074.1:g.517655C>T , LRG_267:g.517655C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000524961.6:n.1889C>T (SBF2)
ENST00000529587.2:n.399C>T (SBF2)
ENST00000675281.2:c.5480C>T (SBF2) ENSP00000502491.1:p.Pro1827Leu
ENST00000676324.2:c.*1713C>T (SBF2) ENSP00000502578.1:n.*1713C>T
ENST00000676387.2:c.5462C>T (SBF2) ENSP00000502779.1:p.Pro1821Leu
ENST00000688344.1:c.5012C>T (SBF2) ENSP00000509987.1:p.Pro1671Leu
ENST00000689128.1:c.5501C>T (SBF2) ENSP00000509587.1:p.Pro1834Leu
ENST00000689258.1:c.5342C>T (SBF2) ENSP00000510475.1:p.Pro1781Leu
ENST00000689342.1:c.1571C>T (SBF2)
ENST00000689356.1:n.2576C>T (SBF2)
ENST00000689940.1:c.5399C>T (SBF2) ENSP00000508452.1:p.Pro1800Leu
ENST00000690437.1:n.1354C>T (SBF2)
ENST00000690944.1:c.1485C>T (SBF2)
ENST00000691616.1:n.1881C>T (SBF2)
ENST00000692716.1:c.5276C>T (SBF2) ENSP00000509545.1:p.Pro1759Leu
ENST00000693541.1:n.2324C>T (SBF2)
ENST00000256190.13:c.5405C>T (SBF2) MANE Select ENSP00000256190.8:p.Pro1802Leu
ENST00000675281.1:c.5480C>T (SBF2) ENSP00000502491.1:p.Pro1827Leu
ENST00000676324.1:c.*1713C>T (SBF2) ENSP00000502578.1:n.*1713C>T
ENST00000676387.1:c.5462C>T (SBF2) ENSP00000502779.1:p.Pro1821Leu
ENST00000256190.12:c.5405C>T (SBF2) ENSP00000256190.8:p.Pro1802Leu
ENST00000525040.5:n.708C>T (SBF2)
ENST00000529587.1:n.399C>T (SBF2)
ENST00000617179.4:c.5264C>T (SBF2) ENSP00000482806.1:p.Pro1755Leu
NM_030962.3:c.5405C>T , LRG_267t1:c.5405C>T (SBF2) NP_112224.1:p.Pro1802Leu
NR_036485.1:n.211+23050G>A (SBF2-AS1)
XM_005253154.3:c.5501C>T (SBF2) XP_005253211.1:p.Pro1834Leu
XM_005253155.3:c.5372C>T (SBF2) XP_005253212.1:p.Pro1791Leu
XM_011520394.1:c.5387C>T (SBF2) XP_011518696.1:p.Pro1796Leu
XR_931024.1:n.200+978G>A
XR_931025.1:n.200+978G>A
XM_005253154.5:c.5501C>T (SBF2) XP_005253211.1:p.Pro1834Leu
XM_005253155.5:c.5372C>T (SBF2) XP_005253212.1:p.Pro1791Leu
XM_011520394.3:c.5387C>T (SBF2) XP_011518696.1:p.Pro1796Leu
XM_017018372.2:c.5363C>T (SBF2) XP_016873861.1:p.Pro1788Leu
XM_017018373.2:c.5363C>T (SBF2) XP_016873862.1:p.Pro1788Leu
XM_017018374.2:c.5276C>T (SBF2) XP_016873863.1:p.Pro1759Leu
XM_017018375.2:c.5264C>T (SBF2) XP_016873864.1:p.Pro1755Leu
XR_001747994.2:n.5512C>T (SBF2)
XR_001748470.1:n.200+978G>A
XR_001748471.1:n.85+978G>A
NM_001386339.1:c.5501C>T (SBF2) NP_001373268.1:p.Pro1834Leu
NM_001386342.1:c.5276C>T (SBF2) NP_001373271.1:p.Pro1759Leu
NM_030962.4:c.5405C>T (SBF2) MANE Select NP_112224.1:p.Pro1802Leu