Canonical Allele Identifier: CA1675523488
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201366A= , CM000668.2:g.157201366A= GRCh38
NC_000006.11:g.157522500A= , CM000668.1:g.157522500A= GRCh37
NC_000006.10:g.157564192A= NCBI36
NG_032093.1:g.428437A=
NG_032093.2:g.428437A=
NG_066624.1:g.430341A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.4982A= ENSP00000055163.8:p.Gln1661=
ENST00000414678.8:c.5051A= ENSP00000412835.3:p.Gln1684=
ENST00000637015.2:c.5270A= ENSP00000489729.2:p.Gln1757=
ENST00000346085.10:c.5021A= ENSP00000344546.5:p.Gln1674=
ENST00000350026.10:c.4733A= ENSP00000055163.7:p.Gln1578=
ENST00000414678.7:c.3299A= ENSP00000412835.2:p.Gln1100=
ENST00000635849.1:c.2462A= ENSP00000490948.1:p.Gln821=
ENST00000635957.1:c.2093A= ENSP00000490385.1:p.Gln698=
ENST00000636227.1:n.3604A=
ENST00000636254.1:n.1061A=
ENST00000636930.2:c.5141A= MANE Select ENSP00000490491.2:p.Gln1714=
ENST00000636940.1:n.3138A=
ENST00000637015.1:c.2509A=
ENST00000637568.1:c.2423A=
ENST00000637741.1:n.1807A=
ENST00000637810.1:c.2483A= ENSP00000489636.1:p.Gln828=
ENST00000637904.1:c.2642A= ENSP00000490550.1:p.Gln881=
ENST00000647938.1:c.4772A= ENSP00000498155.1:p.Gln1591=
ENST00000346085.9:c.4772A= ENSP00000344546.4:p.Gln1591=
ENST00000350026.9:c.4733A= ENSP00000055163.7:p.Gln1578=
ENST00000414678.6:c.3299A= ENSP00000412835.2:p.Gln1100=
NM_017519.2:c.4733A= NP_059989.2:p.Gln1578=
NM_020732.3:c.4772A= NP_065783.3:p.Gln1591=
XM_005267069.3:c.4892A= XP_005267126.2:p.Gln1631=
XM_011535984.1:c.3971A= XP_011534286.1:p.Gln1324=
XM_011535985.1:c.3791A= XP_011534287.1:p.Gln1264=
XM_011535986.1:c.3551A= XP_011534288.1:p.Gln1184=
XM_011535987.1:c.3170A= XP_011534289.1:p.Gln1057=
XM_011535988.1:c.2033A= XP_011534290.1:p.Gln678=
NM_001346813.1:c.4892A= NP_001333742.1:p.Gln1631=
NM_001363725.1:c.2642A= NP_001350654.1:p.Gln881=
XM_011535984.2:c.5102A= XP_011534286.2:p.Gln1701=
XM_011535988.3:c.2033A= XP_011534290.1:p.Gln678=
XM_017011103.2:c.5003A= XP_016866592.1:p.Gln1668=
XM_017011104.1:c.4973A= XP_016866593.1:p.Gln1658=
XM_017011105.2:c.4943A= XP_016866594.1:p.Gln1648=
XM_017011106.2:c.4814A= XP_016866595.1:p.Gln1605=
XM_017011107.2:c.4793A= XP_016866596.1:p.Gln1598=
XR_002956289.1:n.5088A=
NM_001363725.2:c.2642A= NP_001350654.1:p.Gln881=
NM_001371656.1:c.5021A= NP_001358585.1:p.Gln1674=
NM_001374820.1:c.5021A= NP_001361749.1:p.Gln1674=
NM_001374828.1:c.5141A= MANE Select NP_001361757.1:p.Gln1714=
NM_017519.3:c.4982A= NP_059989.3:p.Gln1661=