Canonical Allele Identifier: CA366234082

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510818C>T (hg19) ; chr6:g.157189684C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189684C>T , CM000668.2:g.157189684C>T	GRCh38
NC_000006.11:g.157510818C>T , CM000668.1:g.157510818C>T	GRCh37
NC_000006.10:g.157552510C>T	NCBI36
NG_032093.1:g.416755C>T
NG_032093.2:g.416755C>T
NG_066624.1:g.418659C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3803C>T	ENSP00000055163.8:p.Thr1268Ile
ENST00000414678.8:c.3872C>T	ENSP00000412835.3:p.Thr1291Ile
ENST00000637015.2:c.4091C>T	ENSP00000489729.2:p.Thr1364Ile
ENST00000346085.10:c.3842C>T	ENSP00000344546.5:p.Thr1281Ile
ENST00000350026.10:c.3554C>T	ENSP00000055163.7:p.Thr1185Ile
ENST00000414678.7:c.2120C>T	ENSP00000412835.2:p.Thr707Ile
ENST00000635849.1:c.1283C>T	ENSP00000490948.1:p.Thr428Ile
ENST00000635957.1:c.917C>T	ENSP00000490385.1:p.Thr306Ile
ENST00000636930.2:c.3962C>T MANE Select	ENSP00000490491.2:p.Thr1321Ile
ENST00000636940.1:n.1959C>T
ENST00000637015.1:c.1330C>T
ENST00000637568.1:c.1244C>T
ENST00000637741.1:n.628C>T
ENST00000637810.1:c.1304C>T	ENSP00000489636.1:p.Thr435Ile
ENST00000637904.1:c.1463C>T	ENSP00000490550.1:p.Thr488Ile
ENST00000647938.1:c.3593C>T	ENSP00000498155.1:p.Thr1198Ile
ENST00000346085.9:c.3593C>T	ENSP00000344546.4:p.Thr1198Ile
ENST00000350026.9:c.3554C>T	ENSP00000055163.7:p.Thr1185Ile
ENST00000414678.6:c.2120C>T	ENSP00000412835.2:p.Thr707Ile
NM_017519.2:c.3554C>T	NP_059989.2:p.Thr1185Ile
NM_020732.3:c.3593C>T	NP_065783.3:p.Thr1198Ile
XM_005267069.3:c.3713C>T	XP_005267126.2:p.Thr1238Ile
XM_011535984.1:c.2792C>T	XP_011534286.1:p.Thr931Ile
XM_011535985.1:c.2612C>T	XP_011534287.1:p.Thr871Ile
XM_011535986.1:c.2372C>T	XP_011534288.1:p.Thr791Ile
XM_011535987.1:c.1991C>T	XP_011534289.1:p.Thr664Ile
XM_011535988.1:c.854C>T	XP_011534290.1:p.Thr285Ile
NM_001346813.1:c.3713C>T	NP_001333742.1:p.Thr1238Ile
NM_001363725.1:c.1463C>T	NP_001350654.1:p.Thr488Ile
XM_011535984.2:c.3923C>T	XP_011534286.2:p.Thr1308Ile
XM_011535988.3:c.854C>T	XP_011534290.1:p.Thr285Ile
XM_017011103.2:c.3824C>T	XP_016866592.1:p.Thr1275Ile
XM_017011104.1:c.3794C>T	XP_016866593.1:p.Thr1265Ile
XM_017011105.2:c.3764C>T	XP_016866594.1:p.Thr1255Ile
XM_017011106.2:c.3635C>T	XP_016866595.1:p.Thr1212Ile
XM_017011107.2:c.3614C>T	XP_016866596.1:p.Thr1205Ile
XR_002956289.1:n.4006C>T
NM_001363725.2:c.1463C>T	NP_001350654.1:p.Thr488Ile
NM_001371656.1:c.3842C>T	NP_001358585.1:p.Thr1281Ile
NM_001374820.1:c.3842C>T	NP_001361749.1:p.Thr1281Ile
NM_001374828.1:c.3962C>T MANE Select	NP_001361757.1:p.Thr1321Ile
NM_017519.3:c.3803C>T	NP_059989.3:p.Thr1268Ile