Canonical Allele Identifier: CA366241306

Gene: ARID1B

Linked Data

• dbSNP Id: rs750713205
• MyVariant Identifiers: chr6:g.157522091T>A (hg19) ; chr6:g.157200957T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200957T>A , CM000668.2:g.157200957T>A	GRCh38
NC_000006.11:g.157522091T>A , CM000668.1:g.157522091T>A	GRCh37
NC_000006.10:g.157563783T>A	NCBI36
NG_032093.1:g.428028T>A
NG_032093.2:g.428028T>A
NG_066624.1:g.429932T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4573T>A	ENSP00000055163.8:p.Ser1525Thr
ENST00000414678.8:c.4642T>A	ENSP00000412835.3:p.Ser1548Thr
ENST00000637015.2:c.4861T>A	ENSP00000489729.2:p.Ser1621Thr
ENST00000346085.10:c.4612T>A	ENSP00000344546.5:p.Ser1538Thr
ENST00000350026.10:c.4324T>A	ENSP00000055163.7:p.Ser1442Thr
ENST00000414678.7:c.2890T>A	ENSP00000412835.2:p.Ser964Thr
ENST00000635849.1:c.2053T>A	ENSP00000490948.1:p.Ser685Thr
ENST00000635957.1:c.1684T>A	ENSP00000490385.1:p.Ser562Thr
ENST00000636227.1:n.3195T>A
ENST00000636254.1:n.652T>A
ENST00000636930.2:c.4732T>A MANE Select	ENSP00000490491.2:p.Ser1578Thr
ENST00000636940.1:n.2729T>A
ENST00000637015.1:c.2100T>A
ENST00000637568.1:c.2014T>A
ENST00000637741.1:n.1398T>A
ENST00000637810.1:c.2074T>A	ENSP00000489636.1:p.Ser692Thr
ENST00000637904.1:c.2233T>A	ENSP00000490550.1:p.Ser745Thr
ENST00000647938.1:c.4363T>A	ENSP00000498155.1:p.Ser1455Thr
ENST00000346085.9:c.4363T>A	ENSP00000344546.4:p.Ser1455Thr
ENST00000350026.9:c.4324T>A	ENSP00000055163.7:p.Ser1442Thr
ENST00000414678.6:c.2890T>A	ENSP00000412835.2:p.Ser964Thr
NM_017519.2:c.4324T>A	NP_059989.2:p.Ser1442Thr
NM_020732.3:c.4363T>A	NP_065783.3:p.Ser1455Thr
XM_005267069.3:c.4483T>A	XP_005267126.2:p.Ser1495Thr
XM_011535984.1:c.3562T>A	XP_011534286.1:p.Ser1188Thr
XM_011535985.1:c.3382T>A	XP_011534287.1:p.Ser1128Thr
XM_011535986.1:c.3142T>A	XP_011534288.1:p.Ser1048Thr
XM_011535987.1:c.2761T>A	XP_011534289.1:p.Ser921Thr
XM_011535988.1:c.1624T>A	XP_011534290.1:p.Ser542Thr
NM_001346813.1:c.4483T>A	NP_001333742.1:p.Ser1495Thr
NM_001363725.1:c.2233T>A	NP_001350654.1:p.Ser745Thr
XM_011535984.2:c.4693T>A	XP_011534286.2:p.Ser1565Thr
XM_011535988.3:c.1624T>A	XP_011534290.1:p.Ser542Thr
XM_017011103.2:c.4594T>A	XP_016866592.1:p.Ser1532Thr
XM_017011104.1:c.4564T>A	XP_016866593.1:p.Ser1522Thr
XM_017011105.2:c.4534T>A	XP_016866594.1:p.Ser1512Thr
XM_017011106.2:c.4405T>A	XP_016866595.1:p.Ser1469Thr
XM_017011107.2:c.4384T>A	XP_016866596.1:p.Ser1462Thr
XR_002956289.1:n.4679T>A
NM_001363725.2:c.2233T>A	NP_001350654.1:p.Ser745Thr
NM_001371656.1:c.4612T>A	NP_001358585.1:p.Ser1538Thr
NM_001374820.1:c.4612T>A	NP_001361749.1:p.Ser1538Thr
NM_001374828.1:c.4732T>A MANE Select	NP_001361757.1:p.Ser1578Thr
NM_017519.3:c.4573T>A	NP_059989.3:p.Ser1525Thr