Canonical Allele Identifier: CA1675534246

Gene: ARID1B

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3438C=	ENSP00000055163.8:p.Tyr1146=
ENST00000414678.8:c.3507C=	ENSP00000412835.3:p.Tyr1169=
ENST00000637015.2:c.3726C=	ENSP00000489729.2:p.Tyr1242=
ENST00000319584.11:c.1611C=	ENSP00000313006.7:p.Tyr537=
ENST00000346085.10:c.3477C=	ENSP00000344546.5:p.Tyr1159=
ENST00000350026.10:c.3189C=	ENSP00000055163.7:p.Tyr1063=
ENST00000414678.7:c.1755C=	ENSP00000412835.2:p.Tyr585=
ENST00000635849.1:c.918C=	ENSP00000490948.1:p.Tyr306=
ENST00000635957.1:c.552C=	ENSP00000490385.1:p.Tyr184=
ENST00000636930.2:c.3597C= MANE Select	ENSP00000490491.2:p.Tyr1199=
ENST00000636940.1:n.1594C=
ENST00000637015.1:c.965C=
ENST00000637568.1:c.879C=
ENST00000637741.1:n.263C=
ENST00000637810.1:c.939C=	ENSP00000489636.1:p.Tyr313=
ENST00000637904.1:c.1098C=	ENSP00000490550.1:p.Tyr366=
ENST00000647938.1:c.3228C=	ENSP00000498155.1:p.Tyr1076=
ENST00000319584.10:c.1614C=	ENSP00000313006.6:p.Tyr538=
ENST00000346085.9:c.3228C=	ENSP00000344546.4:p.Tyr1076=
ENST00000350026.9:c.3189C=	ENSP00000055163.7:p.Tyr1063=
ENST00000400790.3:c.390C=	ENSP00000383596.3:p.Tyr130=
ENST00000414678.6:c.1755C=	ENSP00000412835.2:p.Tyr585=
ENST00000478761.3:c.799C=
NM_017519.2:c.3189C=	NP_059989.2:p.Tyr1063=
NM_020732.3:c.3228C=	NP_065783.3:p.Tyr1076=
XM_005267069.3:c.3348C=	XP_005267126.2:p.Tyr1116=
XM_011535984.1:c.2427C=	XP_011534286.1:p.Tyr809=
XM_011535985.1:c.2247C=	XP_011534287.1:p.Tyr749=
XM_011535986.1:c.2007C=	XP_011534288.1:p.Tyr669=
XM_011535987.1:c.1626C=	XP_011534289.1:p.Tyr542=
XM_011535988.1:c.489C=	XP_011534290.1:p.Tyr163=
NM_001346813.1:c.3348C=	NP_001333742.1:p.Tyr1116=
NM_001363725.1:c.1098C=	NP_001350654.1:p.Tyr366=
XM_011535984.2:c.3558C=	XP_011534286.2:p.Tyr1186=
XM_011535988.3:c.489C=	XP_011534290.1:p.Tyr163=
XM_017011103.2:c.3459C=	XP_016866592.1:p.Tyr1153=
XM_017011104.1:c.3429C=	XP_016866593.1:p.Tyr1143=
XM_017011105.2:c.3399C=	XP_016866594.1:p.Tyr1133=
XM_017011106.2:c.3270C=	XP_016866595.1:p.Tyr1090=
XM_017011107.2:c.3249C=	XP_016866596.1:p.Tyr1083=
XR_002956289.1:n.3641C=
NM_001363725.2:c.1098C=	NP_001350654.1:p.Tyr366=
NM_001371656.1:c.3477C=	NP_001358585.1:p.Tyr1159=
NM_001374820.1:c.3477C=	NP_001361749.1:p.Tyr1159=
NM_001374828.1:c.3597C= MANE Select	NP_001361757.1:p.Tyr1199=
NM_017519.3:c.3438C=	NP_059989.3:p.Tyr1146=