Canonical Allele Identifier: CA366241493

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522146A>G (hg19) ; chr6:g.157201012A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201012A>G , CM000668.2:g.157201012A>G	GRCh38
NC_000006.11:g.157522146A>G , CM000668.1:g.157522146A>G	GRCh37
NC_000006.10:g.157563838A>G	NCBI36
NG_032093.1:g.428083A>G
NG_032093.2:g.428083A>G
NG_066624.1:g.429987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4628A>G	ENSP00000055163.8:p.Tyr1543Cys
ENST00000414678.8:c.4697A>G	ENSP00000412835.3:p.Tyr1566Cys
ENST00000637015.2:c.4916A>G	ENSP00000489729.2:p.Tyr1639Cys
ENST00000346085.10:c.4667A>G	ENSP00000344546.5:p.Tyr1556Cys
ENST00000350026.10:c.4379A>G	ENSP00000055163.7:p.Tyr1460Cys
ENST00000414678.7:c.2945A>G	ENSP00000412835.2:p.Tyr982Cys
ENST00000635849.1:c.2108A>G	ENSP00000490948.1:p.Tyr703Cys
ENST00000635957.1:c.1739A>G	ENSP00000490385.1:p.Tyr580Cys
ENST00000636227.1:n.3250A>G
ENST00000636254.1:n.707A>G
ENST00000636930.2:c.4787A>G MANE Select	ENSP00000490491.2:p.Tyr1596Cys
ENST00000636940.1:n.2784A>G
ENST00000637015.1:c.2155A>G
ENST00000637568.1:c.2069A>G
ENST00000637741.1:n.1453A>G
ENST00000637810.1:c.2129A>G	ENSP00000489636.1:p.Tyr710Cys
ENST00000637904.1:c.2288A>G	ENSP00000490550.1:p.Tyr763Cys
ENST00000647938.1:c.4418A>G	ENSP00000498155.1:p.Tyr1473Cys
ENST00000346085.9:c.4418A>G	ENSP00000344546.4:p.Tyr1473Cys
ENST00000350026.9:c.4379A>G	ENSP00000055163.7:p.Tyr1460Cys
ENST00000414678.6:c.2945A>G	ENSP00000412835.2:p.Tyr982Cys
NM_017519.2:c.4379A>G	NP_059989.2:p.Tyr1460Cys
NM_020732.3:c.4418A>G	NP_065783.3:p.Tyr1473Cys
XM_005267069.3:c.4538A>G	XP_005267126.2:p.Tyr1513Cys
XM_011535984.1:c.3617A>G	XP_011534286.1:p.Tyr1206Cys
XM_011535985.1:c.3437A>G	XP_011534287.1:p.Tyr1146Cys
XM_011535986.1:c.3197A>G	XP_011534288.1:p.Tyr1066Cys
XM_011535987.1:c.2816A>G	XP_011534289.1:p.Tyr939Cys
XM_011535988.1:c.1679A>G	XP_011534290.1:p.Tyr560Cys
NM_001346813.1:c.4538A>G	NP_001333742.1:p.Tyr1513Cys
NM_001363725.1:c.2288A>G	NP_001350654.1:p.Tyr763Cys
XM_011535984.2:c.4748A>G	XP_011534286.2:p.Tyr1583Cys
XM_011535988.3:c.1679A>G	XP_011534290.1:p.Tyr560Cys
XM_017011103.2:c.4649A>G	XP_016866592.1:p.Tyr1550Cys
XM_017011104.1:c.4619A>G	XP_016866593.1:p.Tyr1540Cys
XM_017011105.2:c.4589A>G	XP_016866594.1:p.Tyr1530Cys
XM_017011106.2:c.4460A>G	XP_016866595.1:p.Tyr1487Cys
XM_017011107.2:c.4439A>G	XP_016866596.1:p.Tyr1480Cys
XR_002956289.1:n.4734A>G
NM_001363725.2:c.2288A>G	NP_001350654.1:p.Tyr763Cys
NM_001371656.1:c.4667A>G	NP_001358585.1:p.Tyr1556Cys
NM_001374820.1:c.4667A>G	NP_001361749.1:p.Tyr1556Cys
NM_001374828.1:c.4787A>G MANE Select	NP_001361757.1:p.Tyr1596Cys
NM_017519.3:c.4628A>G	NP_059989.3:p.Tyr1543Cys