Canonical Allele Identifier: CA366241757
Gene: ARID1B HGNC NCBI

Linked Data

dbSNP Id: rs1467542976

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157201059C>T , CM000668.2:g.157201059C>T GRCh38
NC_000006.11:g.157522193C>T , CM000668.1:g.157522193C>T GRCh37
NC_000006.10:g.157563885C>T NCBI36
NG_032093.1:g.428130C>T
NG_032093.2:g.428130C>T
NG_066624.1:g.430034C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.4675C>T ENSP00000055163.8:p.Pro1559Ser
ENST00000414678.8:c.4744C>T ENSP00000412835.3:p.Pro1582Ser
ENST00000637015.2:c.4963C>T ENSP00000489729.2:p.Pro1655Ser
ENST00000346085.10:c.4714C>T ENSP00000344546.5:p.Pro1572Ser
ENST00000350026.10:c.4426C>T ENSP00000055163.7:p.Pro1476Ser
ENST00000414678.7:c.2992C>T ENSP00000412835.2:p.Pro998Ser
ENST00000635849.1:c.2155C>T ENSP00000490948.1:p.Pro719Ser
ENST00000635957.1:c.1786C>T ENSP00000490385.1:p.Pro596Ser
ENST00000636227.1:n.3297C>T
ENST00000636254.1:n.754C>T
ENST00000636930.2:c.4834C>T MANE Select ENSP00000490491.2:p.Pro1612Ser
ENST00000636940.1:n.2831C>T
ENST00000637015.1:c.2202C>T
ENST00000637568.1:c.2116C>T
ENST00000637741.1:n.1500C>T
ENST00000637810.1:c.2176C>T ENSP00000489636.1:p.Pro726Ser
ENST00000637904.1:c.2335C>T ENSP00000490550.1:p.Pro779Ser
ENST00000647938.1:c.4465C>T ENSP00000498155.1:p.Pro1489Ser
ENST00000346085.9:c.4465C>T ENSP00000344546.4:p.Pro1489Ser
ENST00000350026.9:c.4426C>T ENSP00000055163.7:p.Pro1476Ser
ENST00000414678.6:c.2992C>T ENSP00000412835.2:p.Pro998Ser
NM_017519.2:c.4426C>T NP_059989.2:p.Pro1476Ser
NM_020732.3:c.4465C>T NP_065783.3:p.Pro1489Ser
XM_005267069.3:c.4585C>T XP_005267126.2:p.Pro1529Ser
XM_011535984.1:c.3664C>T XP_011534286.1:p.Pro1222Ser
XM_011535985.1:c.3484C>T XP_011534287.1:p.Pro1162Ser
XM_011535986.1:c.3244C>T XP_011534288.1:p.Pro1082Ser
XM_011535987.1:c.2863C>T XP_011534289.1:p.Pro955Ser
XM_011535988.1:c.1726C>T XP_011534290.1:p.Pro576Ser
NM_001346813.1:c.4585C>T NP_001333742.1:p.Pro1529Ser
NM_001363725.1:c.2335C>T NP_001350654.1:p.Pro779Ser
XM_011535984.2:c.4795C>T XP_011534286.2:p.Pro1599Ser
XM_011535988.3:c.1726C>T XP_011534290.1:p.Pro576Ser
XM_017011103.2:c.4696C>T XP_016866592.1:p.Pro1566Ser
XM_017011104.1:c.4666C>T XP_016866593.1:p.Pro1556Ser
XM_017011105.2:c.4636C>T XP_016866594.1:p.Pro1546Ser
XM_017011106.2:c.4507C>T XP_016866595.1:p.Pro1503Ser
XM_017011107.2:c.4486C>T XP_016866596.1:p.Pro1496Ser
XR_002956289.1:n.4781C>T
NM_001363725.2:c.2335C>T NP_001350654.1:p.Pro779Ser
NM_001371656.1:c.4714C>T NP_001358585.1:p.Pro1572Ser
NM_001374820.1:c.4714C>T NP_001361749.1:p.Pro1572Ser
NM_001374828.1:c.4834C>T MANE Select NP_001361757.1:p.Pro1612Ser
NM_017519.3:c.4675C>T NP_059989.3:p.Pro1559Ser