Canonical Allele Identifier: CA366240918

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157200781-A-G
• MyVariant Identifiers: chr6:g.157521915A>G (hg19) ; chr6:g.157200781A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200781A>G , CM000668.2:g.157200781A>G	GRCh38
NC_000006.11:g.157521915A>G , CM000668.1:g.157521915A>G	GRCh37
NC_000006.10:g.157563607A>G	NCBI36
NG_032093.1:g.427852A>G
NG_032093.2:g.427852A>G
NG_066624.1:g.429756A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4397A>G	ENSP00000055163.8:p.Tyr1466Cys
ENST00000414678.8:c.4466A>G	ENSP00000412835.3:p.Tyr1489Cys
ENST00000637015.2:c.4685A>G	ENSP00000489729.2:p.Tyr1562Cys
ENST00000346085.10:c.4436A>G	ENSP00000344546.5:p.Tyr1479Cys
ENST00000350026.10:c.4148A>G	ENSP00000055163.7:p.Tyr1383Cys
ENST00000414678.7:c.2714A>G	ENSP00000412835.2:p.Tyr905Cys
ENST00000635849.1:c.1877A>G	ENSP00000490948.1:p.Tyr626Cys
ENST00000635957.1:c.1508A>G	ENSP00000490385.1:p.Tyr503Cys
ENST00000636227.1:n.3019A>G
ENST00000636254.1:n.476A>G
ENST00000636930.2:c.4556A>G MANE Select	ENSP00000490491.2:p.Tyr1519Cys
ENST00000636940.1:n.2553A>G
ENST00000637015.1:c.1924A>G
ENST00000637568.1:c.1838A>G
ENST00000637741.1:n.1222A>G
ENST00000637810.1:c.1898A>G	ENSP00000489636.1:p.Tyr633Cys
ENST00000637904.1:c.2057A>G	ENSP00000490550.1:p.Tyr686Cys
ENST00000647938.1:c.4187A>G	ENSP00000498155.1:p.Tyr1396Cys
ENST00000346085.9:c.4187A>G	ENSP00000344546.4:p.Tyr1396Cys
ENST00000350026.9:c.4148A>G	ENSP00000055163.7:p.Tyr1383Cys
ENST00000414678.6:c.2714A>G	ENSP00000412835.2:p.Tyr905Cys
NM_017519.2:c.4148A>G	NP_059989.2:p.Tyr1383Cys
NM_020732.3:c.4187A>G	NP_065783.3:p.Tyr1396Cys
XM_005267069.3:c.4307A>G	XP_005267126.2:p.Tyr1436Cys
XM_011535984.1:c.3386A>G	XP_011534286.1:p.Tyr1129Cys
XM_011535985.1:c.3206A>G	XP_011534287.1:p.Tyr1069Cys
XM_011535986.1:c.2966A>G	XP_011534288.1:p.Tyr989Cys
XM_011535987.1:c.2585A>G	XP_011534289.1:p.Tyr862Cys
XM_011535988.1:c.1448A>G	XP_011534290.1:p.Tyr483Cys
NM_001346813.1:c.4307A>G	NP_001333742.1:p.Tyr1436Cys
NM_001363725.1:c.2057A>G	NP_001350654.1:p.Tyr686Cys
XM_011535984.2:c.4517A>G	XP_011534286.2:p.Tyr1506Cys
XM_011535988.3:c.1448A>G	XP_011534290.1:p.Tyr483Cys
XM_017011103.2:c.4418A>G	XP_016866592.1:p.Tyr1473Cys
XM_017011104.1:c.4388A>G	XP_016866593.1:p.Tyr1463Cys
XM_017011105.2:c.4358A>G	XP_016866594.1:p.Tyr1453Cys
XM_017011106.2:c.4229A>G	XP_016866595.1:p.Tyr1410Cys
XM_017011107.2:c.4208A>G	XP_016866596.1:p.Tyr1403Cys
XR_002956289.1:n.4503A>G
NM_001363725.2:c.2057A>G	NP_001350654.1:p.Tyr686Cys
NM_001371656.1:c.4436A>G	NP_001358585.1:p.Tyr1479Cys
NM_001374820.1:c.4436A>G	NP_001361749.1:p.Tyr1479Cys
NM_001374828.1:c.4556A>G MANE Select	NP_001361757.1:p.Tyr1519Cys
NM_017519.3:c.4397A>G	NP_059989.3:p.Tyr1466Cys