Canonical Allele Identifier: CA366235295

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511245A>T (hg19) ; chr6:g.157190111A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190111A>T , CM000668.2:g.157190111A>T	GRCh38
NC_000006.11:g.157511245A>T , CM000668.1:g.157511245A>T	GRCh37
NC_000006.10:g.157552937A>T	NCBI36
NG_032093.1:g.417182A>T
NG_032093.2:g.417182A>T
NG_066624.1:g.419086A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3973A>T	ENSP00000055163.8:p.Thr1325Ser
ENST00000414678.8:c.4042A>T	ENSP00000412835.3:p.Thr1348Ser
ENST00000637015.2:c.4261A>T	ENSP00000489729.2:p.Thr1421Ser
ENST00000346085.10:c.4012A>T	ENSP00000344546.5:p.Thr1338Ser
ENST00000350026.10:c.3724A>T	ENSP00000055163.7:p.Thr1242Ser
ENST00000414678.7:c.2290A>T	ENSP00000412835.2:p.Thr764Ser
ENST00000635849.1:c.1453A>T	ENSP00000490948.1:p.Thr485Ser
ENST00000635957.1:c.1084A>T	ENSP00000490385.1:p.Thr362Ser
ENST00000636930.2:c.4132A>T MANE Select	ENSP00000490491.2:p.Thr1378Ser
ENST00000636940.1:n.2129A>T
ENST00000637015.1:c.1500A>T
ENST00000637568.1:c.1414A>T
ENST00000637741.1:n.798A>T
ENST00000637810.1:c.1474A>T	ENSP00000489636.1:p.Thr492Ser
ENST00000637904.1:c.1633A>T	ENSP00000490550.1:p.Thr545Ser
ENST00000647938.1:c.3763A>T	ENSP00000498155.1:p.Thr1255Ser
ENST00000346085.9:c.3763A>T	ENSP00000344546.4:p.Thr1255Ser
ENST00000350026.9:c.3724A>T	ENSP00000055163.7:p.Thr1242Ser
ENST00000414678.6:c.2290A>T	ENSP00000412835.2:p.Thr764Ser
NM_017519.2:c.3724A>T	NP_059989.2:p.Thr1242Ser
NM_020732.3:c.3763A>T	NP_065783.3:p.Thr1255Ser
XM_005267069.3:c.3883A>T	XP_005267126.2:p.Thr1295Ser
XM_011535984.1:c.2962A>T	XP_011534286.1:p.Thr988Ser
XM_011535985.1:c.2782A>T	XP_011534287.1:p.Thr928Ser
XM_011535986.1:c.2542A>T	XP_011534288.1:p.Thr848Ser
XM_011535987.1:c.2161A>T	XP_011534289.1:p.Thr721Ser
XM_011535988.1:c.1024A>T	XP_011534290.1:p.Thr342Ser
NM_001346813.1:c.3883A>T	NP_001333742.1:p.Thr1295Ser
NM_001363725.1:c.1633A>T	NP_001350654.1:p.Thr545Ser
XM_011535984.2:c.4093A>T	XP_011534286.2:p.Thr1365Ser
XM_011535988.3:c.1024A>T	XP_011534290.1:p.Thr342Ser
XM_017011103.2:c.3994A>T	XP_016866592.1:p.Thr1332Ser
XM_017011104.1:c.3964A>T	XP_016866593.1:p.Thr1322Ser
XM_017011105.2:c.3934A>T	XP_016866594.1:p.Thr1312Ser
XM_017011106.2:c.3805A>T	XP_016866595.1:p.Thr1269Ser
XM_017011107.2:c.3784A>T	XP_016866596.1:p.Thr1262Ser
XR_002956289.1:n.4176A>T
NM_001363725.2:c.1633A>T	NP_001350654.1:p.Thr545Ser
NM_001371656.1:c.4012A>T	NP_001358585.1:p.Thr1338Ser
NM_001374820.1:c.4012A>T	NP_001361749.1:p.Thr1338Ser
NM_001374828.1:c.4132A>T MANE Select	NP_001361757.1:p.Thr1378Ser
NM_017519.3:c.3973A>T	NP_059989.3:p.Thr1325Ser