Canonical Allele Identifier: CA10316297
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50455464C>T , CM000684.2:g.50455464C>T GRCh38
NC_000022.10:g.50893893C>T , CM000684.1:g.50893893C>T GRCh37
NC_000022.9:g.49240759C>T NCBI36
NG_041810.1:g.24608G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.4290+17G>A ENSP00000252027.8:n.4290+17G>A
ENST00000470434.2:n.690+17G>A
ENST00000684986.1:c.4371+17G>A ENSP00000509117.1:n.4371+17G>A
ENST00000685180.1:n.2488+5070G>A
ENST00000685390.1:n.2336+17G>A
ENST00000685411.1:n.37+17G>A
ENST00000685592.1:c.602+17G>A
ENST00000685809.1:c.4281+17G>A ENSP00000508863.1:n.4281+17G>A
ENST00000686029.1:c.464+17G>A
ENST00000686191.1:n.3568+17G>A
ENST00000686222.1:c.*3790+17G>A ENSP00000508737.1:n.*3790+17G>A
ENST00000686321.1:c.464+17G>A
ENST00000686427.1:c.*1303+17G>A ENSP00000510379.1:n.*1303+17G>A
ENST00000686758.1:n.2030+17G>A
ENST00000686801.1:c.4356+17G>A ENSP00000509915.1:n.4356+17G>A
ENST00000686826.1:n.687+15G>A
ENST00000687016.1:c.4269+17G>A ENSP00000509074.1:n.4269+17G>A
ENST00000687704.1:c.*2093+17G>A ENSP00000510454.1:n.*2093+17G>A
ENST00000688066.1:c.4368+17G>A ENSP00000510782.1:n.4368+17G>A
ENST00000688124.1:c.*3286+15G>A ENSP00000510645.1:n.*3286+15G>A
ENST00000688848.1:c.*3712+17G>A ENSP00000509419.1:n.*3712+17G>A
ENST00000688985.1:c.1369+17G>A ENSP00000510477.1:n.1369+17G>A
ENST00000689129.1:c.4293+17G>A ENSP00000510414.1:n.4293+17G>A
ENST00000689177.1:n.5640+17G>A
ENST00000689849.1:c.464+17G>A
ENST00000689981.1:c.4368+17G>A ENSP00000509035.1:n.4368+17G>A
ENST00000690369.1:n.4386+17G>A
ENST00000690590.1:n.1415+17G>A
ENST00000690990.1:c.4362+17G>A ENSP00000510461.1:n.4362+17G>A
ENST00000691233.1:c.4287+17G>A ENSP00000509215.1:n.4287+17G>A
ENST00000691306.1:c.466+15G>A
ENST00000691345.1:n.2302+752G>A
ENST00000691792.1:c.4368+17G>A ENSP00000509911.1:n.4368+17G>A
ENST00000691959.1:n.5087+17G>A
ENST00000692844.1:n.1452+17G>A
ENST00000692946.1:c.464+17G>A
ENST00000693052.1:c.4386+17G>A ENSP00000509558.1:n.4386+17G>A
ENST00000693289.1:n.1527+17G>A
ENST00000693440.1:c.4365+17G>A ENSP00000509462.1:n.4365+17G>A
ENST00000693499.1:n.5293+17G>A
ENST00000693591.1:n.3105+17G>A
ENST00000380817.8:c.4368+17G>A MANE Select ENSP00000370196.2:n.4368+17G>A
ENST00000348911.10:c.4293+17G>A ENSP00000252027.7:n.4293+17G>A
ENST00000380817.7:c.4368+17G>A ENSP00000370196.2:n.4368+17G>A
ENST00000470434.1:n.509+17G>A
NM_002972.3:c.4368+17G>A NP_002963.2:n.4368+17G>A
XM_005261931.1:c.4371+17G>A XP_005261988.1:n.4371+17G>A
XM_005261935.1:c.4290+17G>A XP_005261992.1:n.4290+17G>A
XM_011530707.1:c.4470+17G>A XP_011529009.1:n.4470+17G>A
XM_011530708.1:c.4422+17G>A XP_011529010.1:n.4422+17G>A
XM_011530709.1:c.4398+17G>A XP_011529011.1:n.4398+17G>A
XM_011530710.1:c.4395+17G>A XP_011529012.1:n.4395+17G>A
XM_011530711.1:c.4395+17G>A XP_011529013.1:n.4395+17G>A
XR_938344.1:n.4488+17G>A
NM_001365819.1:c.4293+17G>A NP_001352748.1:n.4293+17G>A
XM_005261935.2:c.4290+17G>A XP_005261992.1:n.4290+17G>A
XM_011530709.2:c.4398+17G>A XP_011529011.1:n.4398+17G>A
XM_011530710.2:c.4395+17G>A XP_011529012.1:n.4395+17G>A
XM_017028905.2:c.4320+17G>A XP_016884394.1:n.4320+17G>A
NM_002972.4:c.4368+17G>A MANE Select NP_002963.2:n.4368+17G>A