Canonical Allele Identifier: CA1675538384
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190049T= , CM000668.2:g.157190049T= GRCh38
NC_000006.11:g.157511183T= , CM000668.1:g.157511183T= GRCh37
NC_000006.10:g.157552875T= NCBI36
NG_032093.1:g.417120T=
NG_032093.2:g.417120T=
NG_066624.1:g.419024T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3911T= ENSP00000055163.8:p.Ile1304=
ENST00000414678.8:c.3980T= ENSP00000412835.3:p.Ile1327=
ENST00000637015.2:c.4199T= ENSP00000489729.2:p.Ile1400=
ENST00000346085.10:c.3950T= ENSP00000344546.5:p.Ile1317=
ENST00000350026.10:c.3662T= ENSP00000055163.7:p.Ile1221=
ENST00000414678.7:c.2228T= ENSP00000412835.2:p.Ile743=
ENST00000635849.1:c.1391T= ENSP00000490948.1:p.Ile464=
ENST00000635957.1:c.1022T= ENSP00000490385.1:p.Ile341=
ENST00000636930.2:c.4070T= MANE Select ENSP00000490491.2:p.Ile1357=
ENST00000636940.1:n.2067T=
ENST00000637015.1:c.1438T=
ENST00000637568.1:c.1352T=
ENST00000637741.1:n.736T=
ENST00000637810.1:c.1412T= ENSP00000489636.1:p.Ile471=
ENST00000637904.1:c.1571T= ENSP00000490550.1:p.Ile524=
ENST00000647938.1:c.3701T= ENSP00000498155.1:p.Ile1234=
ENST00000346085.9:c.3701T= ENSP00000344546.4:p.Ile1234=
ENST00000350026.9:c.3662T= ENSP00000055163.7:p.Ile1221=
ENST00000414678.6:c.2228T= ENSP00000412835.2:p.Ile743=
NM_017519.2:c.3662T= NP_059989.2:p.Ile1221=
NM_020732.3:c.3701T= NP_065783.3:p.Ile1234=
XM_005267069.3:c.3821T= XP_005267126.2:p.Ile1274=
XM_011535984.1:c.2900T= XP_011534286.1:p.Ile967=
XM_011535985.1:c.2720T= XP_011534287.1:p.Ile907=
XM_011535986.1:c.2480T= XP_011534288.1:p.Ile827=
XM_011535987.1:c.2099T= XP_011534289.1:p.Ile700=
XM_011535988.1:c.962T= XP_011534290.1:p.Ile321=
NM_001346813.1:c.3821T= NP_001333742.1:p.Ile1274=
NM_001363725.1:c.1571T= NP_001350654.1:p.Ile524=
XM_011535984.2:c.4031T= XP_011534286.2:p.Ile1344=
XM_011535988.3:c.962T= XP_011534290.1:p.Ile321=
XM_017011103.2:c.3932T= XP_016866592.1:p.Ile1311=
XM_017011104.1:c.3902T= XP_016866593.1:p.Ile1301=
XM_017011105.2:c.3872T= XP_016866594.1:p.Ile1291=
XM_017011106.2:c.3743T= XP_016866595.1:p.Ile1248=
XM_017011107.2:c.3722T= XP_016866596.1:p.Ile1241=
XR_002956289.1:n.4114T=
NM_001363725.2:c.1571T= NP_001350654.1:p.Ile524=
NM_001371656.1:c.3950T= NP_001358585.1:p.Ile1317=
NM_001374820.1:c.3950T= NP_001361749.1:p.Ile1317=
NM_001374828.1:c.4070T= MANE Select NP_001361757.1:p.Ile1357=
NM_017519.3:c.3911T= NP_059989.3:p.Ile1304=