Canonical Allele Identifier: CA366242239
Gene: ARID1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201206C>A , CM000668.2:g.157201206C>A GRCh38
NC_000006.11:g.157522340C>A , CM000668.1:g.157522340C>A GRCh37
NC_000006.10:g.157564032C>A NCBI36
NG_032093.1:g.428277C>A
NG_032093.2:g.428277C>A
NG_066624.1:g.430181C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4822C>A ENSP00000055163.8:p.Pro1608Thr
ENST00000414678.8:c.4891C>A ENSP00000412835.3:p.Pro1631Thr
ENST00000637015.2:c.5110C>A ENSP00000489729.2:p.Pro1704Thr
ENST00000346085.10:c.4861C>A ENSP00000344546.5:p.Pro1621Thr
ENST00000350026.10:c.4573C>A ENSP00000055163.7:p.Pro1525Thr
ENST00000414678.7:c.3139C>A ENSP00000412835.2:p.Pro1047Thr
ENST00000635849.1:c.2302C>A ENSP00000490948.1:p.Pro768Thr
ENST00000635957.1:c.1933C>A ENSP00000490385.1:p.Pro645Thr
ENST00000636227.1:n.3444C>A
ENST00000636254.1:n.901C>A
ENST00000636930.2:c.4981C>A MANE Select ENSP00000490491.2:p.Pro1661Thr
ENST00000636940.1:n.2978C>A
ENST00000637015.1:c.2349C>A
ENST00000637568.1:c.2263C>A
ENST00000637741.1:n.1647C>A
ENST00000637810.1:c.2323C>A ENSP00000489636.1:p.Pro775Thr
ENST00000637904.1:c.2482C>A ENSP00000490550.1:p.Pro828Thr
ENST00000647938.1:c.4612C>A ENSP00000498155.1:p.Pro1538Thr
ENST00000346085.9:c.4612C>A ENSP00000344546.4:p.Pro1538Thr
ENST00000350026.9:c.4573C>A ENSP00000055163.7:p.Pro1525Thr
ENST00000414678.6:c.3139C>A ENSP00000412835.2:p.Pro1047Thr
NM_017519.2:c.4573C>A NP_059989.2:p.Pro1525Thr
NM_020732.3:c.4612C>A NP_065783.3:p.Pro1538Thr
XM_005267069.3:c.4732C>A XP_005267126.2:p.Pro1578Thr
XM_011535984.1:c.3811C>A XP_011534286.1:p.Pro1271Thr
XM_011535985.1:c.3631C>A XP_011534287.1:p.Pro1211Thr
XM_011535986.1:c.3391C>A XP_011534288.1:p.Pro1131Thr
XM_011535987.1:c.3010C>A XP_011534289.1:p.Pro1004Thr
XM_011535988.1:c.1873C>A XP_011534290.1:p.Pro625Thr
NM_001346813.1:c.4732C>A NP_001333742.1:p.Pro1578Thr
NM_001363725.1:c.2482C>A NP_001350654.1:p.Pro828Thr
XM_011535984.2:c.4942C>A XP_011534286.2:p.Pro1648Thr
XM_011535988.3:c.1873C>A XP_011534290.1:p.Pro625Thr
XM_017011103.2:c.4843C>A XP_016866592.1:p.Pro1615Thr
XM_017011104.1:c.4813C>A XP_016866593.1:p.Pro1605Thr
XM_017011105.2:c.4783C>A XP_016866594.1:p.Pro1595Thr
XM_017011106.2:c.4654C>A XP_016866595.1:p.Pro1552Thr
XM_017011107.2:c.4633C>A XP_016866596.1:p.Pro1545Thr
XR_002956289.1:n.4928C>A
NM_001363725.2:c.2482C>A NP_001350654.1:p.Pro828Thr
NM_001371656.1:c.4861C>A NP_001358585.1:p.Pro1621Thr
NM_001374820.1:c.4861C>A NP_001361749.1:p.Pro1621Thr
NM_001374828.1:c.4981C>A MANE Select NP_001361757.1:p.Pro1661Thr
NM_017519.3:c.4822C>A NP_059989.3:p.Pro1608Thr