Canonical Allele Identifier: CA1675538243
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157189688C= , CM000668.2:g.157189688C= GRCh38
NC_000006.11:g.157510822C= , CM000668.1:g.157510822C= GRCh37
NC_000006.10:g.157552514C= NCBI36
NG_032093.1:g.416759C=
NG_032093.2:g.416759C=
NG_066624.1:g.418663C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3807C= ENSP00000055163.8:p.Gly1269=
ENST00000414678.8:c.3876C= ENSP00000412835.3:p.Gly1292=
ENST00000637015.2:c.4095C= ENSP00000489729.2:p.Gly1365=
ENST00000346085.10:c.3846C= ENSP00000344546.5:p.Gly1282=
ENST00000350026.10:c.3558C= ENSP00000055163.7:p.Gly1186=
ENST00000414678.7:c.2124C= ENSP00000412835.2:p.Gly708=
ENST00000635849.1:c.1287C= ENSP00000490948.1:p.Gly429=
ENST00000635957.1:c.921C= ENSP00000490385.1:p.Gly307=
ENST00000636930.2:c.3966C= MANE Select ENSP00000490491.2:p.Gly1322=
ENST00000636940.1:n.1963C=
ENST00000637015.1:c.1334C=
ENST00000637568.1:c.1248C=
ENST00000637741.1:n.632C=
ENST00000637810.1:c.1308C= ENSP00000489636.1:p.Gly436=
ENST00000637904.1:c.1467C= ENSP00000490550.1:p.Gly489=
ENST00000647938.1:c.3597C= ENSP00000498155.1:p.Gly1199=
ENST00000346085.9:c.3597C= ENSP00000344546.4:p.Gly1199=
ENST00000350026.9:c.3558C= ENSP00000055163.7:p.Gly1186=
ENST00000414678.6:c.2124C= ENSP00000412835.2:p.Gly708=
NM_017519.2:c.3558C= NP_059989.2:p.Gly1186=
NM_020732.3:c.3597C= NP_065783.3:p.Gly1199=
XM_005267069.3:c.3717C= XP_005267126.2:p.Gly1239=
XM_011535984.1:c.2796C= XP_011534286.1:p.Gly932=
XM_011535985.1:c.2616C= XP_011534287.1:p.Gly872=
XM_011535986.1:c.2376C= XP_011534288.1:p.Gly792=
XM_011535987.1:c.1995C= XP_011534289.1:p.Gly665=
XM_011535988.1:c.858C= XP_011534290.1:p.Gly286=
NM_001346813.1:c.3717C= NP_001333742.1:p.Gly1239=
NM_001363725.1:c.1467C= NP_001350654.1:p.Gly489=
XM_011535984.2:c.3927C= XP_011534286.2:p.Gly1309=
XM_011535988.3:c.858C= XP_011534290.1:p.Gly286=
XM_017011103.2:c.3828C= XP_016866592.1:p.Gly1276=
XM_017011104.1:c.3798C= XP_016866593.1:p.Gly1266=
XM_017011105.2:c.3768C= XP_016866594.1:p.Gly1256=
XM_017011106.2:c.3639C= XP_016866595.1:p.Gly1213=
XM_017011107.2:c.3618C= XP_016866596.1:p.Gly1206=
XR_002956289.1:n.4010C=
NM_001363725.2:c.1467C= NP_001350654.1:p.Gly489=
NM_001371656.1:c.3846C= NP_001358585.1:p.Gly1282=
NM_001374820.1:c.3846C= NP_001361749.1:p.Gly1282=
NM_001374828.1:c.3966C= MANE Select NP_001361757.1:p.Gly1322=
NM_017519.3:c.3807C= NP_059989.3:p.Gly1269=