Canonical Allele Identifier: CA1675522923
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201068G= , CM000668.2:g.157201068G= GRCh38
NC_000006.11:g.157522202G= , CM000668.1:g.157522202G= GRCh37
NC_000006.10:g.157563894G= NCBI36
NG_032093.1:g.428139G=
NG_032093.2:g.428139G=
NG_066624.1:g.430043G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4684G= ENSP00000055163.8:p.Gly1562=
ENST00000414678.8:c.4753G= ENSP00000412835.3:p.Gly1585=
ENST00000637015.2:c.4972G= ENSP00000489729.2:p.Gly1658=
ENST00000346085.10:c.4723G= ENSP00000344546.5:p.Gly1575=
ENST00000350026.10:c.4435G= ENSP00000055163.7:p.Gly1479=
ENST00000414678.7:c.3001G= ENSP00000412835.2:p.Gly1001=
ENST00000635849.1:c.2164G= ENSP00000490948.1:p.Gly722=
ENST00000635957.1:c.1795G= ENSP00000490385.1:p.Gly599=
ENST00000636227.1:n.3306G=
ENST00000636254.1:n.763G=
ENST00000636930.2:c.4843G= MANE Select ENSP00000490491.2:p.Gly1615=
ENST00000636940.1:n.2840G=
ENST00000637015.1:c.2211G=
ENST00000637568.1:c.2125G=
ENST00000637741.1:n.1509G=
ENST00000637810.1:c.2185G= ENSP00000489636.1:p.Gly729=
ENST00000637904.1:c.2344G= ENSP00000490550.1:p.Gly782=
ENST00000647938.1:c.4474G= ENSP00000498155.1:p.Gly1492=
ENST00000346085.9:c.4474G= ENSP00000344546.4:p.Gly1492=
ENST00000350026.9:c.4435G= ENSP00000055163.7:p.Gly1479=
ENST00000414678.6:c.3001G= ENSP00000412835.2:p.Gly1001=
NM_017519.2:c.4435G= NP_059989.2:p.Gly1479=
NM_020732.3:c.4474G= NP_065783.3:p.Gly1492=
XM_005267069.3:c.4594G= XP_005267126.2:p.Gly1532=
XM_011535984.1:c.3673G= XP_011534286.1:p.Gly1225=
XM_011535985.1:c.3493G= XP_011534287.1:p.Gly1165=
XM_011535986.1:c.3253G= XP_011534288.1:p.Gly1085=
XM_011535987.1:c.2872G= XP_011534289.1:p.Gly958=
XM_011535988.1:c.1735G= XP_011534290.1:p.Gly579=
NM_001346813.1:c.4594G= NP_001333742.1:p.Gly1532=
NM_001363725.1:c.2344G= NP_001350654.1:p.Gly782=
XM_011535984.2:c.4804G= XP_011534286.2:p.Gly1602=
XM_011535988.3:c.1735G= XP_011534290.1:p.Gly579=
XM_017011103.2:c.4705G= XP_016866592.1:p.Gly1569=
XM_017011104.1:c.4675G= XP_016866593.1:p.Gly1559=
XM_017011105.2:c.4645G= XP_016866594.1:p.Gly1549=
XM_017011106.2:c.4516G= XP_016866595.1:p.Gly1506=
XM_017011107.2:c.4495G= XP_016866596.1:p.Gly1499=
XR_002956289.1:n.4790G=
NM_001363725.2:c.2344G= NP_001350654.1:p.Gly782=
NM_001371656.1:c.4723G= NP_001358585.1:p.Gly1575=
NM_001374820.1:c.4723G= NP_001361749.1:p.Gly1575=
NM_001374828.1:c.4843G= MANE Select NP_001361757.1:p.Gly1615=
NM_017519.3:c.4684G= NP_059989.3:p.Gly1562=