Canonical Allele Identifier: CA1675538222
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189648C= , CM000668.2:g.157189648C= GRCh38
NC_000006.11:g.157510782C= , CM000668.1:g.157510782C= GRCh37
NC_000006.10:g.157552474C= NCBI36
NG_032093.1:g.416719C=
NG_032093.2:g.416719C=
NG_066624.1:g.418623C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3767C= ENSP00000055163.8:p.Ser1256=
ENST00000414678.8:c.3836C= ENSP00000412835.3:p.Ser1279=
ENST00000637015.2:c.4055C= ENSP00000489729.2:p.Ser1352=
ENST00000346085.10:c.3806C= ENSP00000344546.5:p.Ser1269=
ENST00000350026.10:c.3518C= ENSP00000055163.7:p.Ser1173=
ENST00000414678.7:c.2084C= ENSP00000412835.2:p.Ser695=
ENST00000635849.1:c.1247C= ENSP00000490948.1:p.Ser416=
ENST00000635957.1:c.881C= ENSP00000490385.1:p.Ser294=
ENST00000636930.2:c.3926C= MANE Select ENSP00000490491.2:p.Ser1309=
ENST00000636940.1:n.1923C=
ENST00000637015.1:c.1294C=
ENST00000637568.1:c.1208C=
ENST00000637741.1:n.592C=
ENST00000637810.1:c.1268C= ENSP00000489636.1:p.Ser423=
ENST00000637904.1:c.1427C= ENSP00000490550.1:p.Ser476=
ENST00000647938.1:c.3557C= ENSP00000498155.1:p.Ser1186=
ENST00000346085.9:c.3557C= ENSP00000344546.4:p.Ser1186=
ENST00000350026.9:c.3518C= ENSP00000055163.7:p.Ser1173=
ENST00000414678.6:c.2084C= ENSP00000412835.2:p.Ser695=
NM_017519.2:c.3518C= NP_059989.2:p.Ser1173=
NM_020732.3:c.3557C= NP_065783.3:p.Ser1186=
XM_005267069.3:c.3677C= XP_005267126.2:p.Ser1226=
XM_011535984.1:c.2756C= XP_011534286.1:p.Ser919=
XM_011535985.1:c.2576C= XP_011534287.1:p.Ser859=
XM_011535986.1:c.2336C= XP_011534288.1:p.Ser779=
XM_011535987.1:c.1955C= XP_011534289.1:p.Ser652=
XM_011535988.1:c.818C= XP_011534290.1:p.Ser273=
NM_001346813.1:c.3677C= NP_001333742.1:p.Ser1226=
NM_001363725.1:c.1427C= NP_001350654.1:p.Ser476=
XM_011535984.2:c.3887C= XP_011534286.2:p.Ser1296=
XM_011535988.3:c.818C= XP_011534290.1:p.Ser273=
XM_017011103.2:c.3788C= XP_016866592.1:p.Ser1263=
XM_017011104.1:c.3758C= XP_016866593.1:p.Ser1253=
XM_017011105.2:c.3728C= XP_016866594.1:p.Ser1243=
XM_017011106.2:c.3599C= XP_016866595.1:p.Ser1200=
XM_017011107.2:c.3578C= XP_016866596.1:p.Ser1193=
XR_002956289.1:n.3970C=
NM_001363725.2:c.1427C= NP_001350654.1:p.Ser476=
NM_001371656.1:c.3806C= NP_001358585.1:p.Ser1269=
NM_001374820.1:c.3806C= NP_001361749.1:p.Ser1269=
NM_001374828.1:c.3926C= MANE Select NP_001361757.1:p.Ser1309=
NM_017519.3:c.3767C= NP_059989.3:p.Ser1256=