Canonical Allele Identifier: CA366243111

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201443C>T , CM000668.2:g.157201443C>T	GRCh38
NC_000006.11:g.157522577C>T , CM000668.1:g.157522577C>T	GRCh37
NC_000006.10:g.157564269C>T	NCBI36
NG_032093.1:g.428514C>T
NG_032093.2:g.428514C>T
NG_066624.1:g.430418C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5059C>T	ENSP00000055163.8:p.Gln1687Ter
ENST00000414678.8:c.5128C>T	ENSP00000412835.3:p.Gln1710Ter
ENST00000637015.2:c.5347C>T	ENSP00000489729.2:p.Gln1783Ter
ENST00000346085.10:c.5098C>T	ENSP00000344546.5:p.Gln1700Ter
ENST00000350026.10:c.4810C>T	ENSP00000055163.7:p.Gln1604Ter
ENST00000414678.7:c.3376C>T	ENSP00000412835.2:p.Gln1126Ter
ENST00000635849.1:c.2539C>T	ENSP00000490948.1:p.Gln847Ter
ENST00000635957.1:c.2170C>T	ENSP00000490385.1:p.Gln724Ter
ENST00000636227.1:n.3681C>T
ENST00000636254.1:n.1138C>T
ENST00000636930.2:c.5218C>T MANE Select	ENSP00000490491.2:p.Gln1740Ter
ENST00000636940.1:n.3215C>T
ENST00000637015.1:c.2586C>T
ENST00000637568.1:c.2500C>T
ENST00000637741.1:n.1884C>T
ENST00000637810.1:c.2560C>T	ENSP00000489636.1:p.Gln854Ter
ENST00000637904.1:c.2719C>T	ENSP00000490550.1:p.Gln907Ter
ENST00000647938.1:c.4849C>T	ENSP00000498155.1:p.Gln1617Ter
ENST00000346085.9:c.4849C>T	ENSP00000344546.4:p.Gln1617Ter
ENST00000350026.9:c.4810C>T	ENSP00000055163.7:p.Gln1604Ter
ENST00000414678.6:c.3376C>T	ENSP00000412835.2:p.Gln1126Ter
NM_017519.2:c.4810C>T	NP_059989.2:p.Gln1604Ter
NM_020732.3:c.4849C>T	NP_065783.3:p.Gln1617Ter
XM_005267069.3:c.4969C>T	XP_005267126.2:p.Gln1657Ter
XM_011535984.1:c.4048C>T	XP_011534286.1:p.Gln1350Ter
XM_011535985.1:c.3868C>T	XP_011534287.1:p.Gln1290Ter
XM_011535986.1:c.3628C>T	XP_011534288.1:p.Gln1210Ter
XM_011535987.1:c.3247C>T	XP_011534289.1:p.Gln1083Ter
XM_011535988.1:c.2110C>T	XP_011534290.1:p.Gln704Ter
NM_001346813.1:c.4969C>T	NP_001333742.1:p.Gln1657Ter
NM_001363725.1:c.2719C>T	NP_001350654.1:p.Gln907Ter
XM_011535984.2:c.5179C>T	XP_011534286.2:p.Gln1727Ter
XM_011535988.3:c.2110C>T	XP_011534290.1:p.Gln704Ter
XM_017011103.2:c.5080C>T	XP_016866592.1:p.Gln1694Ter
XM_017011104.1:c.5050C>T	XP_016866593.1:p.Gln1684Ter
XM_017011105.2:c.5020C>T	XP_016866594.1:p.Gln1674Ter
XM_017011106.2:c.4891C>T	XP_016866595.1:p.Gln1631Ter
XM_017011107.2:c.4870C>T	XP_016866596.1:p.Gln1624Ter
XR_002956289.1:n.5165C>T
NM_001363725.2:c.2719C>T	NP_001350654.1:p.Gln907Ter
NM_001371656.1:c.5098C>T	NP_001358585.1:p.Gln1700Ter
NM_001374820.1:c.5098C>T	NP_001361749.1:p.Gln1700Ter
NM_001374828.1:c.5218C>T MANE Select	NP_001361757.1:p.Gln1740Ter
NM_017519.3:c.5059C>T	NP_059989.3:p.Gln1687Ter