Canonical Allele Identifier: CA1675538380
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190041C= , CM000668.2:g.157190041C= GRCh38
NC_000006.11:g.157511175C= , CM000668.1:g.157511175C= GRCh37
NC_000006.10:g.157552867C= NCBI36
NG_032093.1:g.417112C=
NG_032093.2:g.417112C=
NG_066624.1:g.419016C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3903C= ENSP00000055163.8:p.Ser1301=
ENST00000414678.8:c.3972C= ENSP00000412835.3:p.Ser1324=
ENST00000637015.2:c.4191C= ENSP00000489729.2:p.Ser1397=
ENST00000346085.10:c.3942C= ENSP00000344546.5:p.Ser1314=
ENST00000350026.10:c.3654C= ENSP00000055163.7:p.Ser1218=
ENST00000414678.7:c.2220C= ENSP00000412835.2:p.Ser740=
ENST00000635849.1:c.1383C= ENSP00000490948.1:p.Ser461=
ENST00000635957.1:c.1014C= ENSP00000490385.1:p.Ser338=
ENST00000636930.2:c.4062C= MANE Select ENSP00000490491.2:p.Ser1354=
ENST00000636940.1:n.2059C=
ENST00000637015.1:c.1430C=
ENST00000637568.1:c.1344C=
ENST00000637741.1:n.728C=
ENST00000637810.1:c.1404C= ENSP00000489636.1:p.Ser468=
ENST00000637904.1:c.1563C= ENSP00000490550.1:p.Ser521=
ENST00000647938.1:c.3693C= ENSP00000498155.1:p.Ser1231=
ENST00000346085.9:c.3693C= ENSP00000344546.4:p.Ser1231=
ENST00000350026.9:c.3654C= ENSP00000055163.7:p.Ser1218=
ENST00000414678.6:c.2220C= ENSP00000412835.2:p.Ser740=
NM_017519.2:c.3654C= NP_059989.2:p.Ser1218=
NM_020732.3:c.3693C= NP_065783.3:p.Ser1231=
XM_005267069.3:c.3813C= XP_005267126.2:p.Ser1271=
XM_011535984.1:c.2892C= XP_011534286.1:p.Ser964=
XM_011535985.1:c.2712C= XP_011534287.1:p.Ser904=
XM_011535986.1:c.2472C= XP_011534288.1:p.Ser824=
XM_011535987.1:c.2091C= XP_011534289.1:p.Ser697=
XM_011535988.1:c.954C= XP_011534290.1:p.Ser318=
NM_001346813.1:c.3813C= NP_001333742.1:p.Ser1271=
NM_001363725.1:c.1563C= NP_001350654.1:p.Ser521=
XM_011535984.2:c.4023C= XP_011534286.2:p.Ser1341=
XM_011535988.3:c.954C= XP_011534290.1:p.Ser318=
XM_017011103.2:c.3924C= XP_016866592.1:p.Ser1308=
XM_017011104.1:c.3894C= XP_016866593.1:p.Ser1298=
XM_017011105.2:c.3864C= XP_016866594.1:p.Ser1288=
XM_017011106.2:c.3735C= XP_016866595.1:p.Ser1245=
XM_017011107.2:c.3714C= XP_016866596.1:p.Ser1238=
XR_002956289.1:n.4106C=
NM_001363725.2:c.1563C= NP_001350654.1:p.Ser521=
NM_001371656.1:c.3942C= NP_001358585.1:p.Ser1314=
NM_001374820.1:c.3942C= NP_001361749.1:p.Ser1314=
NM_001374828.1:c.4062C= MANE Select NP_001361757.1:p.Ser1354=
NM_017519.3:c.3903C= NP_059989.3:p.Ser1301=