Canonical Allele Identifier: CA366240822
Community Standard Title: NM_001374828.1(ARID1B):c.4526G>T (p.Arg1509Leu)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157200751G>T , CM000668.2:g.157200751G>T GRCh38
NC_000006.11:g.157521885G>T , CM000668.1:g.157521885G>T GRCh37
NC_000006.10:g.157563577G>T NCBI36
NG_032093.1:g.427822G>T
NG_032093.2:g.427822G>T
NG_066624.1:g.429726G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.4526G>T MANE Select NP_001361757.1:p.Arg1509Leu
ENST00000636930.2:c.4526G>T MANE Select ENSP00000490491.2:p.Arg1509Leu
NM_001346813.1:c.4277G>T NP_001333742.1:p.Arg1426Leu
NM_001363725.1:c.2027G>T NP_001350654.1:p.Arg676Leu
NM_001363725.2:c.2027G>T NP_001350654.1:p.Arg676Leu
NM_001371656.1:c.4406G>T NP_001358585.1:p.Arg1469Leu
NM_001374820.1:c.4406G>T NP_001361749.1:p.Arg1469Leu
NM_017519.2:c.4118G>T NP_059989.2:p.Arg1373Leu
NM_017519.3:c.4367G>T NP_059989.3:p.Arg1456Leu
NM_020732.3:c.4157G>T NP_065783.3:p.Arg1386Leu
ENST00000346085.10:c.4406G>T ENSP00000344546.5:p.Arg1469Leu
ENST00000346085.9:c.4157G>T ENSP00000344546.4:p.Arg1386Leu
ENST00000350026.10:c.4118G>T ENSP00000055163.7:p.Arg1373Leu
ENST00000350026.11:c.4367G>T ENSP00000055163.8:p.Arg1456Leu
ENST00000350026.9:c.4118G>T ENSP00000055163.7:p.Arg1373Leu
ENST00000414678.6:c.2684G>T ENSP00000412835.2:p.Arg895Leu
ENST00000414678.7:c.2684G>T ENSP00000412835.2:p.Arg895Leu
ENST00000414678.8:c.4436G>T ENSP00000412835.3:p.Arg1479Leu
ENST00000635849.1:c.1847G>T ENSP00000490948.1:p.Arg616Leu
ENST00000635957.1:c.1478G>T ENSP00000490385.1:p.Arg493Leu
ENST00000636227.1:n.2989G>T
ENST00000636254.1:n.446G>T
ENST00000636940.1:n.2523G>T
ENST00000637015.1:c.1894G>T
ENST00000637015.2:c.4655G>T ENSP00000489729.2:p.Arg1552Leu
ENST00000637568.1:c.1808G>T
ENST00000637741.1:n.1192G>T
ENST00000637810.1:c.1868G>T ENSP00000489636.1:p.Arg623Leu
ENST00000637904.1:c.2027G>T ENSP00000490550.1:p.Arg676Leu
ENST00000647938.1:c.4157G>T ENSP00000498155.1:p.Arg1386Leu
XM_005267069.3:c.4277G>T XP_005267126.2:p.Arg1426Leu
XM_011535984.1:c.3356G>T XP_011534286.1:p.Arg1119Leu
XM_011535984.2:c.4487G>T XP_011534286.2:p.Arg1496Leu
XM_011535985.1:c.3176G>T XP_011534287.1:p.Arg1059Leu
XM_011535986.1:c.2936G>T XP_011534288.1:p.Arg979Leu
XM_011535987.1:c.2555G>T XP_011534289.1:p.Arg852Leu
XM_011535988.1:c.1418G>T XP_011534290.1:p.Arg473Leu
XM_011535988.3:c.1418G>T XP_011534290.1:p.Arg473Leu
XM_017011103.2:c.4388G>T XP_016866592.1:p.Arg1463Leu
XM_017011104.1:c.4358G>T XP_016866593.1:p.Arg1453Leu
XM_017011105.2:c.4328G>T XP_016866594.1:p.Arg1443Leu
XM_017011106.2:c.4199G>T XP_016866595.1:p.Arg1400Leu
XM_017011107.2:c.4178G>T XP_016866596.1:p.Arg1393Leu
XR_002956289.1:n.4473G>T