Canonical Allele Identifier: CA366234663

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3907A>G	ENSP00000055163.8:p.Thr1303Ala
ENST00000414678.8:c.3976A>G	ENSP00000412835.3:p.Thr1326Ala
ENST00000637015.2:c.4195A>G	ENSP00000489729.2:p.Thr1399Ala
ENST00000346085.10:c.3946A>G	ENSP00000344546.5:p.Thr1316Ala
ENST00000350026.10:c.3658A>G	ENSP00000055163.7:p.Thr1220Ala
ENST00000414678.7:c.2224A>G	ENSP00000412835.2:p.Thr742Ala
ENST00000635849.1:c.1387A>G	ENSP00000490948.1:p.Thr463Ala
ENST00000635957.1:c.1018A>G	ENSP00000490385.1:p.Thr340Ala
ENST00000636930.2:c.4066A>G MANE Select	ENSP00000490491.2:p.Thr1356Ala
ENST00000636940.1:n.2063A>G
ENST00000637015.1:c.1434A>G
ENST00000637568.1:c.1348A>G
ENST00000637741.1:n.732A>G
ENST00000637810.1:c.1408A>G	ENSP00000489636.1:p.Thr470Ala
ENST00000637904.1:c.1567A>G	ENSP00000490550.1:p.Thr523Ala
ENST00000647938.1:c.3697A>G	ENSP00000498155.1:p.Thr1233Ala
ENST00000346085.9:c.3697A>G	ENSP00000344546.4:p.Thr1233Ala
ENST00000350026.9:c.3658A>G	ENSP00000055163.7:p.Thr1220Ala
ENST00000414678.6:c.2224A>G	ENSP00000412835.2:p.Thr742Ala
NM_017519.2:c.3658A>G	NP_059989.2:p.Thr1220Ala
NM_020732.3:c.3697A>G	NP_065783.3:p.Thr1233Ala
XM_005267069.3:c.3817A>G	XP_005267126.2:p.Thr1273Ala
XM_011535984.1:c.2896A>G	XP_011534286.1:p.Thr966Ala
XM_011535985.1:c.2716A>G	XP_011534287.1:p.Thr906Ala
XM_011535986.1:c.2476A>G	XP_011534288.1:p.Thr826Ala
XM_011535987.1:c.2095A>G	XP_011534289.1:p.Thr699Ala
XM_011535988.1:c.958A>G	XP_011534290.1:p.Thr320Ala
NM_001346813.1:c.3817A>G	NP_001333742.1:p.Thr1273Ala
NM_001363725.1:c.1567A>G	NP_001350654.1:p.Thr523Ala
XM_011535984.2:c.4027A>G	XP_011534286.2:p.Thr1343Ala
XM_011535988.3:c.958A>G	XP_011534290.1:p.Thr320Ala
XM_017011103.2:c.3928A>G	XP_016866592.1:p.Thr1310Ala
XM_017011104.1:c.3898A>G	XP_016866593.1:p.Thr1300Ala
XM_017011105.2:c.3868A>G	XP_016866594.1:p.Thr1290Ala
XM_017011106.2:c.3739A>G	XP_016866595.1:p.Thr1247Ala
XM_017011107.2:c.3718A>G	XP_016866596.1:p.Thr1240Ala
XR_002956289.1:n.4110A>G
NM_001363725.2:c.1567A>G	NP_001350654.1:p.Thr523Ala
NM_001371656.1:c.3946A>G	NP_001358585.1:p.Thr1316Ala
NM_001374820.1:c.3946A>G	NP_001361749.1:p.Thr1316Ala
NM_001374828.1:c.4066A>G MANE Select	NP_001361757.1:p.Thr1356Ala
NM_017519.3:c.3907A>G	NP_059989.3:p.Thr1303Ala