Canonical Allele Identifier: CA1675538227
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189657T= , CM000668.2:g.157189657T= GRCh38
NC_000006.11:g.157510791T= , CM000668.1:g.157510791T= GRCh37
NC_000006.10:g.157552483T= NCBI36
NG_032093.1:g.416728T=
NG_032093.2:g.416728T=
NG_066624.1:g.418632T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3776T= ENSP00000055163.8:p.Leu1259=
ENST00000414678.8:c.3845T= ENSP00000412835.3:p.Leu1282=
ENST00000637015.2:c.4064T= ENSP00000489729.2:p.Leu1355=
ENST00000346085.10:c.3815T= ENSP00000344546.5:p.Leu1272=
ENST00000350026.10:c.3527T= ENSP00000055163.7:p.Leu1176=
ENST00000414678.7:c.2093T= ENSP00000412835.2:p.Leu698=
ENST00000635849.1:c.1256T= ENSP00000490948.1:p.Leu419=
ENST00000635957.1:c.890T= ENSP00000490385.1:p.Leu297=
ENST00000636930.2:c.3935T= MANE Select ENSP00000490491.2:p.Leu1312=
ENST00000636940.1:n.1932T=
ENST00000637015.1:c.1303T=
ENST00000637568.1:c.1217T=
ENST00000637741.1:n.601T=
ENST00000637810.1:c.1277T= ENSP00000489636.1:p.Leu426=
ENST00000637904.1:c.1436T= ENSP00000490550.1:p.Leu479=
ENST00000647938.1:c.3566T= ENSP00000498155.1:p.Leu1189=
ENST00000346085.9:c.3566T= ENSP00000344546.4:p.Leu1189=
ENST00000350026.9:c.3527T= ENSP00000055163.7:p.Leu1176=
ENST00000414678.6:c.2093T= ENSP00000412835.2:p.Leu698=
NM_017519.2:c.3527T= NP_059989.2:p.Leu1176=
NM_020732.3:c.3566T= NP_065783.3:p.Leu1189=
XM_005267069.3:c.3686T= XP_005267126.2:p.Leu1229=
XM_011535984.1:c.2765T= XP_011534286.1:p.Leu922=
XM_011535985.1:c.2585T= XP_011534287.1:p.Leu862=
XM_011535986.1:c.2345T= XP_011534288.1:p.Leu782=
XM_011535987.1:c.1964T= XP_011534289.1:p.Leu655=
XM_011535988.1:c.827T= XP_011534290.1:p.Leu276=
NM_001346813.1:c.3686T= NP_001333742.1:p.Leu1229=
NM_001363725.1:c.1436T= NP_001350654.1:p.Leu479=
XM_011535984.2:c.3896T= XP_011534286.2:p.Leu1299=
XM_011535988.3:c.827T= XP_011534290.1:p.Leu276=
XM_017011103.2:c.3797T= XP_016866592.1:p.Leu1266=
XM_017011104.1:c.3767T= XP_016866593.1:p.Leu1256=
XM_017011105.2:c.3737T= XP_016866594.1:p.Leu1246=
XM_017011106.2:c.3608T= XP_016866595.1:p.Leu1203=
XM_017011107.2:c.3587T= XP_016866596.1:p.Leu1196=
XR_002956289.1:n.3979T=
NM_001363725.2:c.1436T= NP_001350654.1:p.Leu479=
NM_001371656.1:c.3815T= NP_001358585.1:p.Leu1272=
NM_001374820.1:c.3815T= NP_001361749.1:p.Leu1272=
NM_001374828.1:c.3935T= MANE Select NP_001361757.1:p.Leu1312=
NM_017519.3:c.3776T= NP_059989.3:p.Leu1259=