Canonical Allele Identifier: CA366234666

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511179A>T (hg19) ; chr6:g.157190045A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190045A>T , CM000668.2:g.157190045A>T	GRCh38
NC_000006.11:g.157511179A>T , CM000668.1:g.157511179A>T	GRCh37
NC_000006.10:g.157552871A>T	NCBI36
NG_032093.1:g.417116A>T
NG_032093.2:g.417116A>T
NG_066624.1:g.419020A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3907A>T	ENSP00000055163.8:p.Thr1303Ser
ENST00000414678.8:c.3976A>T	ENSP00000412835.3:p.Thr1326Ser
ENST00000637015.2:c.4195A>T	ENSP00000489729.2:p.Thr1399Ser
ENST00000346085.10:c.3946A>T	ENSP00000344546.5:p.Thr1316Ser
ENST00000350026.10:c.3658A>T	ENSP00000055163.7:p.Thr1220Ser
ENST00000414678.7:c.2224A>T	ENSP00000412835.2:p.Thr742Ser
ENST00000635849.1:c.1387A>T	ENSP00000490948.1:p.Thr463Ser
ENST00000635957.1:c.1018A>T	ENSP00000490385.1:p.Thr340Ser
ENST00000636930.2:c.4066A>T MANE Select	ENSP00000490491.2:p.Thr1356Ser
ENST00000636940.1:n.2063A>T
ENST00000637015.1:c.1434A>T
ENST00000637568.1:c.1348A>T
ENST00000637741.1:n.732A>T
ENST00000637810.1:c.1408A>T	ENSP00000489636.1:p.Thr470Ser
ENST00000637904.1:c.1567A>T	ENSP00000490550.1:p.Thr523Ser
ENST00000647938.1:c.3697A>T	ENSP00000498155.1:p.Thr1233Ser
ENST00000346085.9:c.3697A>T	ENSP00000344546.4:p.Thr1233Ser
ENST00000350026.9:c.3658A>T	ENSP00000055163.7:p.Thr1220Ser
ENST00000414678.6:c.2224A>T	ENSP00000412835.2:p.Thr742Ser
NM_017519.2:c.3658A>T	NP_059989.2:p.Thr1220Ser
NM_020732.3:c.3697A>T	NP_065783.3:p.Thr1233Ser
XM_005267069.3:c.3817A>T	XP_005267126.2:p.Thr1273Ser
XM_011535984.1:c.2896A>T	XP_011534286.1:p.Thr966Ser
XM_011535985.1:c.2716A>T	XP_011534287.1:p.Thr906Ser
XM_011535986.1:c.2476A>T	XP_011534288.1:p.Thr826Ser
XM_011535987.1:c.2095A>T	XP_011534289.1:p.Thr699Ser
XM_011535988.1:c.958A>T	XP_011534290.1:p.Thr320Ser
NM_001346813.1:c.3817A>T	NP_001333742.1:p.Thr1273Ser
NM_001363725.1:c.1567A>T	NP_001350654.1:p.Thr523Ser
XM_011535984.2:c.4027A>T	XP_011534286.2:p.Thr1343Ser
XM_011535988.3:c.958A>T	XP_011534290.1:p.Thr320Ser
XM_017011103.2:c.3928A>T	XP_016866592.1:p.Thr1310Ser
XM_017011104.1:c.3898A>T	XP_016866593.1:p.Thr1300Ser
XM_017011105.2:c.3868A>T	XP_016866594.1:p.Thr1290Ser
XM_017011106.2:c.3739A>T	XP_016866595.1:p.Thr1247Ser
XM_017011107.2:c.3718A>T	XP_016866596.1:p.Thr1240Ser
XR_002956289.1:n.4110A>T
NM_001363725.2:c.1567A>T	NP_001350654.1:p.Thr523Ser
NM_001371656.1:c.3946A>T	NP_001358585.1:p.Thr1316Ser
NM_001374820.1:c.3946A>T	NP_001361749.1:p.Thr1316Ser
NM_001374828.1:c.4066A>T MANE Select	NP_001361757.1:p.Thr1356Ser
NM_017519.3:c.3907A>T	NP_059989.3:p.Thr1303Ser