Canonical Allele Identifier: CA366241311

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522094T>A (hg19) ; chr6:g.157200960T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200960T>A , CM000668.2:g.157200960T>A	GRCh38
NC_000006.11:g.157522094T>A , CM000668.1:g.157522094T>A	GRCh37
NC_000006.10:g.157563786T>A	NCBI36
NG_032093.1:g.428031T>A
NG_032093.2:g.428031T>A
NG_066624.1:g.429935T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4576T>A	ENSP00000055163.8:p.Ser1526Thr
ENST00000414678.8:c.4645T>A	ENSP00000412835.3:p.Ser1549Thr
ENST00000637015.2:c.4864T>A	ENSP00000489729.2:p.Ser1622Thr
ENST00000346085.10:c.4615T>A	ENSP00000344546.5:p.Ser1539Thr
ENST00000350026.10:c.4327T>A	ENSP00000055163.7:p.Ser1443Thr
ENST00000414678.7:c.2893T>A	ENSP00000412835.2:p.Ser965Thr
ENST00000635849.1:c.2056T>A	ENSP00000490948.1:p.Ser686Thr
ENST00000635957.1:c.1687T>A	ENSP00000490385.1:p.Ser563Thr
ENST00000636227.1:n.3198T>A
ENST00000636254.1:n.655T>A
ENST00000636930.2:c.4735T>A MANE Select	ENSP00000490491.2:p.Ser1579Thr
ENST00000636940.1:n.2732T>A
ENST00000637015.1:c.2103T>A
ENST00000637568.1:c.2017T>A
ENST00000637741.1:n.1401T>A
ENST00000637810.1:c.2077T>A	ENSP00000489636.1:p.Ser693Thr
ENST00000637904.1:c.2236T>A	ENSP00000490550.1:p.Ser746Thr
ENST00000647938.1:c.4366T>A	ENSP00000498155.1:p.Ser1456Thr
ENST00000346085.9:c.4366T>A	ENSP00000344546.4:p.Ser1456Thr
ENST00000350026.9:c.4327T>A	ENSP00000055163.7:p.Ser1443Thr
ENST00000414678.6:c.2893T>A	ENSP00000412835.2:p.Ser965Thr
NM_017519.2:c.4327T>A	NP_059989.2:p.Ser1443Thr
NM_020732.3:c.4366T>A	NP_065783.3:p.Ser1456Thr
XM_005267069.3:c.4486T>A	XP_005267126.2:p.Ser1496Thr
XM_011535984.1:c.3565T>A	XP_011534286.1:p.Ser1189Thr
XM_011535985.1:c.3385T>A	XP_011534287.1:p.Ser1129Thr
XM_011535986.1:c.3145T>A	XP_011534288.1:p.Ser1049Thr
XM_011535987.1:c.2764T>A	XP_011534289.1:p.Ser922Thr
XM_011535988.1:c.1627T>A	XP_011534290.1:p.Ser543Thr
NM_001346813.1:c.4486T>A	NP_001333742.1:p.Ser1496Thr
NM_001363725.1:c.2236T>A	NP_001350654.1:p.Ser746Thr
XM_011535984.2:c.4696T>A	XP_011534286.2:p.Ser1566Thr
XM_011535988.3:c.1627T>A	XP_011534290.1:p.Ser543Thr
XM_017011103.2:c.4597T>A	XP_016866592.1:p.Ser1533Thr
XM_017011104.1:c.4567T>A	XP_016866593.1:p.Ser1523Thr
XM_017011105.2:c.4537T>A	XP_016866594.1:p.Ser1513Thr
XM_017011106.2:c.4408T>A	XP_016866595.1:p.Ser1470Thr
XM_017011107.2:c.4387T>A	XP_016866596.1:p.Ser1463Thr
XR_002956289.1:n.4682T>A
NM_001363725.2:c.2236T>A	NP_001350654.1:p.Ser746Thr
NM_001371656.1:c.4615T>A	NP_001358585.1:p.Ser1539Thr
NM_001374820.1:c.4615T>A	NP_001361749.1:p.Ser1539Thr
NM_001374828.1:c.4735T>A MANE Select	NP_001361757.1:p.Ser1579Thr
NM_017519.3:c.4576T>A	NP_059989.3:p.Ser1526Thr