Canonical Allele Identifier: CA15691319
Gene: SBF2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10500715

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9951515T>G , CM000673.2:g.9951515T>G GRCh38
NC_000011.9:g.9973062T>G , CM000673.1:g.9973062T>G GRCh37
NC_000011.8:g.9929638T>G NCBI36
NG_008074.1:g.347693A>C , LRG_267:g.347693A>C

Transcript Alleles

HGVS Amino-acid change
NM_030962.3:c.1860+10442A>C , LRG_267t1:c.1860+10442A>C NP_112224.1:p.=
XM_005253154.3:c.1860+10442A>C XP_005253211.1:p.=
XM_005253155.3:c.1731+10442A>C XP_005253212.1:p.=
XM_011520394.1:c.1746+10442A>C XP_011518696.1:p.=
XM_011520395.1:c.1860+10442A>C XP_011518697.1:p.=
XM_011520396.1:c.1860+10442A>C XP_011518698.1:p.=
XM_005253154.5:c.1860+10442A>C
XM_005253155.5:c.1731+10442A>C
XM_011520394.3:c.1746+10442A>C
XM_011520395.3:c.1860+10442A>C
XM_011520396.3:c.1860+10442A>C
XM_017018372.2:c.1722+10442A>C XP_016873861.1:p.=
XM_017018373.2:c.1722+10442A>C XP_016873862.1:p.=
XM_017018374.2:c.1731+10442A>C XP_016873863.1:p.=
XM_017018375.2:c.1860+10442A>C XP_016873864.1:p.=
XM_017018376.2:c.1860+10442A>C XP_016873865.1:p.=
XM_017018377.2:c.1860+10442A>C XP_016873866.1:p.=
XR_001747994.2:n.1998+10442A>C
ENST00000256190.12:c.1860+10442A>C ENSP00000256190.8:p.=
ENST00000420722.2:n.679+10442A>C
ENST00000533770.5:n.1775+10442A>C
ENST00000617179.4:n.1719+10442A>C ENSP00000482806.1:p.=