Canonical Allele Identifier: CA1675523506
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201374G= , CM000668.2:g.157201374G= GRCh38
NC_000006.11:g.157522508G= , CM000668.1:g.157522508G= GRCh37
NC_000006.10:g.157564200G= NCBI36
NG_032093.1:g.428445G=
NG_032093.2:g.428445G=
NG_066624.1:g.430349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4990G= ENSP00000055163.8:p.Gly1664=
ENST00000414678.8:c.5059G= ENSP00000412835.3:p.Gly1687=
ENST00000637015.2:c.5278G= ENSP00000489729.2:p.Gly1760=
ENST00000346085.10:c.5029G= ENSP00000344546.5:p.Gly1677=
ENST00000350026.10:c.4741G= ENSP00000055163.7:p.Gly1581=
ENST00000414678.7:c.3307G= ENSP00000412835.2:p.Gly1103=
ENST00000635849.1:c.2470G= ENSP00000490948.1:p.Gly824=
ENST00000635957.1:c.2101G= ENSP00000490385.1:p.Gly701=
ENST00000636227.1:n.3612G=
ENST00000636254.1:n.1069G=
ENST00000636930.2:c.5149G= MANE Select ENSP00000490491.2:p.Gly1717=
ENST00000636940.1:n.3146G=
ENST00000637015.1:c.2517G=
ENST00000637568.1:c.2431G=
ENST00000637741.1:n.1815G=
ENST00000637810.1:c.2491G= ENSP00000489636.1:p.Gly831=
ENST00000637904.1:c.2650G= ENSP00000490550.1:p.Gly884=
ENST00000647938.1:c.4780G= ENSP00000498155.1:p.Gly1594=
ENST00000346085.9:c.4780G= ENSP00000344546.4:p.Gly1594=
ENST00000350026.9:c.4741G= ENSP00000055163.7:p.Gly1581=
ENST00000414678.6:c.3307G= ENSP00000412835.2:p.Gly1103=
NM_017519.2:c.4741G= NP_059989.2:p.Gly1581=
NM_020732.3:c.4780G= NP_065783.3:p.Gly1594=
XM_005267069.3:c.4900G= XP_005267126.2:p.Gly1634=
XM_011535984.1:c.3979G= XP_011534286.1:p.Gly1327=
XM_011535985.1:c.3799G= XP_011534287.1:p.Gly1267=
XM_011535986.1:c.3559G= XP_011534288.1:p.Gly1187=
XM_011535987.1:c.3178G= XP_011534289.1:p.Gly1060=
XM_011535988.1:c.2041G= XP_011534290.1:p.Gly681=
NM_001346813.1:c.4900G= NP_001333742.1:p.Gly1634=
NM_001363725.1:c.2650G= NP_001350654.1:p.Gly884=
XM_011535984.2:c.5110G= XP_011534286.2:p.Gly1704=
XM_011535988.3:c.2041G= XP_011534290.1:p.Gly681=
XM_017011103.2:c.5011G= XP_016866592.1:p.Gly1671=
XM_017011104.1:c.4981G= XP_016866593.1:p.Gly1661=
XM_017011105.2:c.4951G= XP_016866594.1:p.Gly1651=
XM_017011106.2:c.4822G= XP_016866595.1:p.Gly1608=
XM_017011107.2:c.4801G= XP_016866596.1:p.Gly1601=
XR_002956289.1:n.5096G=
NM_001363725.2:c.2650G= NP_001350654.1:p.Gly884=
NM_001371656.1:c.5029G= NP_001358585.1:p.Gly1677=
NM_001374820.1:c.5029G= NP_001361749.1:p.Gly1677=
NM_001374828.1:c.5149G= MANE Select NP_001361757.1:p.Gly1717=
NM_017519.3:c.4990G= NP_059989.3:p.Gly1664=