Canonical Allele Identifier: CA366227645

Gene: ARID1B

Linked Data

• dbSNP Id: rs1562328526
• MyVariant Identifiers: chr6:g.157502195C>A (hg19) ; chr6:g.157181061C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181061C>A , CM000668.2:g.157181061C>A	GRCh38
NC_000006.11:g.157502195C>A , CM000668.1:g.157502195C>A	GRCh37
NC_000006.10:g.157543887C>A	NCBI36
NG_032093.1:g.408132C>A
NG_032093.2:g.408132C>A
NG_066624.1:g.410036C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3438C>A	ENSP00000055163.8:p.Tyr1146Ter
ENST00000414678.8:c.3507C>A	ENSP00000412835.3:p.Tyr1169Ter
ENST00000637015.2:c.3726C>A	ENSP00000489729.2:p.Tyr1242Ter
ENST00000319584.11:c.1611C>A	ENSP00000313006.7:p.Tyr537Ter
ENST00000346085.10:c.3477C>A	ENSP00000344546.5:p.Tyr1159Ter
ENST00000350026.10:c.3189C>A	ENSP00000055163.7:p.Tyr1063Ter
ENST00000414678.7:c.1755C>A	ENSP00000412835.2:p.Tyr585Ter
ENST00000635849.1:c.918C>A	ENSP00000490948.1:p.Tyr306Ter
ENST00000635957.1:c.552C>A	ENSP00000490385.1:p.Tyr184Ter
ENST00000636930.2:c.3597C>A MANE Select	ENSP00000490491.2:p.Tyr1199Ter
ENST00000636940.1:n.1594C>A
ENST00000637015.1:c.965C>A
ENST00000637568.1:c.879C>A
ENST00000637741.1:n.263C>A
ENST00000637810.1:c.939C>A	ENSP00000489636.1:p.Tyr313Ter
ENST00000637904.1:c.1098C>A	ENSP00000490550.1:p.Tyr366Ter
ENST00000647938.1:c.3228C>A	ENSP00000498155.1:p.Tyr1076Ter
ENST00000319584.10:c.1614C>A	ENSP00000313006.6:p.Tyr538Ter
ENST00000346085.9:c.3228C>A	ENSP00000344546.4:p.Tyr1076Ter
ENST00000350026.9:c.3189C>A	ENSP00000055163.7:p.Tyr1063Ter
ENST00000400790.3:c.390C>A	ENSP00000383596.3:p.Tyr130Ter
ENST00000414678.6:c.1755C>A	ENSP00000412835.2:p.Tyr585Ter
ENST00000478761.3:c.799C>A
NM_017519.2:c.3189C>A	NP_059989.2:p.Tyr1063Ter
NM_020732.3:c.3228C>A	NP_065783.3:p.Tyr1076Ter
XM_005267069.3:c.3348C>A	XP_005267126.2:p.Tyr1116Ter
XM_011535984.1:c.2427C>A	XP_011534286.1:p.Tyr809Ter
XM_011535985.1:c.2247C>A	XP_011534287.1:p.Tyr749Ter
XM_011535986.1:c.2007C>A	XP_011534288.1:p.Tyr669Ter
XM_011535987.1:c.1626C>A	XP_011534289.1:p.Tyr542Ter
XM_011535988.1:c.489C>A	XP_011534290.1:p.Tyr163Ter
NM_001346813.1:c.3348C>A	NP_001333742.1:p.Tyr1116Ter
NM_001363725.1:c.1098C>A	NP_001350654.1:p.Tyr366Ter
XM_011535984.2:c.3558C>A	XP_011534286.2:p.Tyr1186Ter
XM_011535988.3:c.489C>A	XP_011534290.1:p.Tyr163Ter
XM_017011103.2:c.3459C>A	XP_016866592.1:p.Tyr1153Ter
XM_017011104.1:c.3429C>A	XP_016866593.1:p.Tyr1143Ter
XM_017011105.2:c.3399C>A	XP_016866594.1:p.Tyr1133Ter
XM_017011106.2:c.3270C>A	XP_016866595.1:p.Tyr1090Ter
XM_017011107.2:c.3249C>A	XP_016866596.1:p.Tyr1083Ter
XR_002956289.1:n.3641C>A
NM_001363725.2:c.1098C>A	NP_001350654.1:p.Tyr366Ter
NM_001371656.1:c.3477C>A	NP_001358585.1:p.Tyr1159Ter
NM_001374820.1:c.3477C>A	NP_001361749.1:p.Tyr1159Ter
NM_001374828.1:c.3597C>A MANE Select	NP_001361757.1:p.Tyr1199Ter
NM_017519.3:c.3438C>A	NP_059989.3:p.Tyr1146Ter