Canonical Allele Identifier: CA10316475
Gene: SBF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50456682G>A , CM000684.2:g.50456682G>A GRCh38
NC_000022.10:g.50895111G>A , CM000684.1:g.50895111G>A GRCh37
NC_000022.9:g.49241977G>A NCBI36
NG_041810.1:g.23390C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000348911.11:c.3827-9C>T ENSP00000252027.8:n.3827-9C>T
ENST00000470434.2:n.227-9C>T
ENST00000684986.1:c.3908-9C>T ENSP00000509117.1:n.3908-9C>T
ENST00000685180.1:n.2488+3852C>T
ENST00000685390.1:n.1873-9C>T
ENST00000685592.1:c.139-9C>T
ENST00000685809.1:c.3818-9C>T ENSP00000508863.1:n.3818-9C>T
ENST00000686191.1:n.3096C>T
ENST00000686222.1:c.*3327-9C>T ENSP00000508737.1:n.*3327-9C>T
ENST00000686427.1:c.*840-9C>T ENSP00000510379.1:n.*840-9C>T
ENST00000686758.1:n.1558C>T
ENST00000686801.1:c.3893-9C>T ENSP00000509915.1:n.3893-9C>T
ENST00000686826.1:n.222-9C>T
ENST00000687016.1:c.3806-9C>T ENSP00000509074.1:n.3806-9C>T
ENST00000687704.1:c.*1630-9C>T ENSP00000510454.1:n.*1630-9C>T
ENST00000688066.1:c.3905-9C>T ENSP00000510782.1:n.3905-9C>T
ENST00000688124.1:c.*2821-9C>T ENSP00000510645.1:n.*2821-9C>T
ENST00000688848.1:c.*3249-9C>T ENSP00000509419.1:n.*3249-9C>T
ENST00000688985.1:c.911-14C>T ENSP00000510477.1:n.911-14C>T
ENST00000689129.1:c.3830-9C>T ENSP00000510414.1:n.3830-9C>T
ENST00000689177.1:n.4535C>T
ENST00000689981.1:c.3905-9C>T ENSP00000509035.1:n.3905-9C>T
ENST00000690369.1:n.3923-9C>T
ENST00000690590.1:n.952-9C>T
ENST00000690990.1:c.3899-9C>T ENSP00000510461.1:n.3899-9C>T
ENST00000691233.1:c.3824-9C>T ENSP00000509215.1:n.3824-9C>T
ENST00000691345.1:n.1941-9C>T
ENST00000691792.1:c.3905-9C>T ENSP00000509911.1:n.3905-9C>T
ENST00000691959.1:n.3991-9C>T
ENST00000692844.1:n.989-9C>T
ENST00000693052.1:c.3923-9C>T ENSP00000509558.1:n.3923-9C>T
ENST00000693289.1:n.1055C>T
ENST00000693440.1:c.3902-9C>T ENSP00000509462.1:n.3902-9C>T
ENST00000693499.1:n.4821C>T
ENST00000693591.1:n.2000C>T
ENST00000380817.8:c.3905-9C>T MANE Select ENSP00000370196.2:n.3905-9C>T
ENST00000348911.10:c.3830-9C>T ENSP00000252027.7:n.3830-9C>T
ENST00000380817.7:c.3905-9C>T ENSP00000370196.2:n.3905-9C>T
ENST00000476293.1:n.315-9C>T
NM_002972.3:c.3905-9C>T NP_002963.2:n.3905-9C>T
XM_005261931.1:c.3908-9C>T XP_005261988.1:n.3908-9C>T
XM_005261935.1:c.3827-9C>T XP_005261992.1:n.3827-9C>T
XM_011530707.1:c.4007-9C>T XP_011529009.1:n.4007-9C>T
XM_011530708.1:c.3959-9C>T XP_011529010.1:n.3959-9C>T
XM_011530709.1:c.3935-9C>T XP_011529011.1:n.3935-9C>T
XM_011530710.1:c.3932-9C>T XP_011529012.1:n.3932-9C>T
XM_011530711.1:c.3932-9C>T XP_011529013.1:n.3932-9C>T
XR_938344.1:n.4025-9C>T
NM_001365819.1:c.3830-9C>T NP_001352748.1:n.3830-9C>T
XM_005261935.2:c.3827-9C>T XP_005261992.1:n.3827-9C>T
XM_011530709.2:c.3935-9C>T XP_011529011.1:n.3935-9C>T
XM_011530710.2:c.3932-9C>T XP_011529012.1:n.3932-9C>T
XM_017028905.2:c.3857-9C>T XP_016884394.1:n.3857-9C>T
NM_002972.4:c.3905-9C>T MANE Select NP_002963.2:n.3905-9C>T