Canonical Allele Identifier: CA1675538387
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190059C= , CM000668.2:g.157190059C= GRCh38
NC_000006.11:g.157511193C= , CM000668.1:g.157511193C= GRCh37
NC_000006.10:g.157552885C= NCBI36
NG_032093.1:g.417130C=
NG_032093.2:g.417130C=
NG_066624.1:g.419034C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3921C= ENSP00000055163.8:p.His1307=
ENST00000414678.8:c.3990C= ENSP00000412835.3:p.His1330=
ENST00000637015.2:c.4209C= ENSP00000489729.2:p.His1403=
ENST00000346085.10:c.3960C= ENSP00000344546.5:p.His1320=
ENST00000350026.10:c.3672C= ENSP00000055163.7:p.His1224=
ENST00000414678.7:c.2238C= ENSP00000412835.2:p.His746=
ENST00000635849.1:c.1401C= ENSP00000490948.1:p.His467=
ENST00000635957.1:c.1032C= ENSP00000490385.1:p.His344=
ENST00000636930.2:c.4080C= MANE Select ENSP00000490491.2:p.His1360=
ENST00000636940.1:n.2077C=
ENST00000637015.1:c.1448C=
ENST00000637568.1:c.1362C=
ENST00000637741.1:n.746C=
ENST00000637810.1:c.1422C= ENSP00000489636.1:p.His474=
ENST00000637904.1:c.1581C= ENSP00000490550.1:p.His527=
ENST00000647938.1:c.3711C= ENSP00000498155.1:p.His1237=
ENST00000346085.9:c.3711C= ENSP00000344546.4:p.His1237=
ENST00000350026.9:c.3672C= ENSP00000055163.7:p.His1224=
ENST00000414678.6:c.2238C= ENSP00000412835.2:p.His746=
NM_017519.2:c.3672C= NP_059989.2:p.His1224=
NM_020732.3:c.3711C= NP_065783.3:p.His1237=
XM_005267069.3:c.3831C= XP_005267126.2:p.His1277=
XM_011535984.1:c.2910C= XP_011534286.1:p.His970=
XM_011535985.1:c.2730C= XP_011534287.1:p.His910=
XM_011535986.1:c.2490C= XP_011534288.1:p.His830=
XM_011535987.1:c.2109C= XP_011534289.1:p.His703=
XM_011535988.1:c.972C= XP_011534290.1:p.His324=
NM_001346813.1:c.3831C= NP_001333742.1:p.His1277=
NM_001363725.1:c.1581C= NP_001350654.1:p.His527=
XM_011535984.2:c.4041C= XP_011534286.2:p.His1347=
XM_011535988.3:c.972C= XP_011534290.1:p.His324=
XM_017011103.2:c.3942C= XP_016866592.1:p.His1314=
XM_017011104.1:c.3912C= XP_016866593.1:p.His1304=
XM_017011105.2:c.3882C= XP_016866594.1:p.His1294=
XM_017011106.2:c.3753C= XP_016866595.1:p.His1251=
XM_017011107.2:c.3732C= XP_016866596.1:p.His1244=
XR_002956289.1:n.4124C=
NM_001363725.2:c.1581C= NP_001350654.1:p.His527=
NM_001371656.1:c.3960C= NP_001358585.1:p.His1320=
NM_001374820.1:c.3960C= NP_001361749.1:p.His1320=
NM_001374828.1:c.4080C= MANE Select NP_001361757.1:p.His1360=
NM_017519.3:c.3921C= NP_059989.3:p.His1307=