Canonical Allele Identifier: CA1675522799

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200989G= , CM000668.2:g.157200989G=	GRCh38
NC_000006.11:g.157522123G= , CM000668.1:g.157522123G=	GRCh37
NC_000006.10:g.157563815G=	NCBI36
NG_032093.1:g.428060G=
NG_032093.2:g.428060G=
NG_066624.1:g.429964G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4605G=	ENSP00000055163.8:p.Trp1535=
ENST00000414678.8:c.4674G=	ENSP00000412835.3:p.Trp1558=
ENST00000637015.2:c.4893G=	ENSP00000489729.2:p.Trp1631=
ENST00000346085.10:c.4644G=	ENSP00000344546.5:p.Trp1548=
ENST00000350026.10:c.4356G=	ENSP00000055163.7:p.Trp1452=
ENST00000414678.7:c.2922G=	ENSP00000412835.2:p.Trp974=
ENST00000635849.1:c.2085G=	ENSP00000490948.1:p.Trp695=
ENST00000635957.1:c.1716G=	ENSP00000490385.1:p.Trp572=
ENST00000636227.1:n.3227G=
ENST00000636254.1:n.684G=
ENST00000636930.2:c.4764G= MANE Select	ENSP00000490491.2:p.Trp1588=
ENST00000636940.1:n.2761G=
ENST00000637015.1:c.2132G=
ENST00000637568.1:c.2046G=
ENST00000637741.1:n.1430G=
ENST00000637810.1:c.2106G=	ENSP00000489636.1:p.Trp702=
ENST00000637904.1:c.2265G=	ENSP00000490550.1:p.Trp755=
ENST00000647938.1:c.4395G=	ENSP00000498155.1:p.Trp1465=
ENST00000346085.9:c.4395G=	ENSP00000344546.4:p.Trp1465=
ENST00000350026.9:c.4356G=	ENSP00000055163.7:p.Trp1452=
ENST00000414678.6:c.2922G=	ENSP00000412835.2:p.Trp974=
NM_017519.2:c.4356G=	NP_059989.2:p.Trp1452=
NM_020732.3:c.4395G=	NP_065783.3:p.Trp1465=
XM_005267069.3:c.4515G=	XP_005267126.2:p.Trp1505=
XM_011535984.1:c.3594G=	XP_011534286.1:p.Trp1198=
XM_011535985.1:c.3414G=	XP_011534287.1:p.Trp1138=
XM_011535986.1:c.3174G=	XP_011534288.1:p.Trp1058=
XM_011535987.1:c.2793G=	XP_011534289.1:p.Trp931=
XM_011535988.1:c.1656G=	XP_011534290.1:p.Trp552=
NM_001346813.1:c.4515G=	NP_001333742.1:p.Trp1505=
NM_001363725.1:c.2265G=	NP_001350654.1:p.Trp755=
XM_011535984.2:c.4725G=	XP_011534286.2:p.Trp1575=
XM_011535988.3:c.1656G=	XP_011534290.1:p.Trp552=
XM_017011103.2:c.4626G=	XP_016866592.1:p.Trp1542=
XM_017011104.1:c.4596G=	XP_016866593.1:p.Trp1532=
XM_017011105.2:c.4566G=	XP_016866594.1:p.Trp1522=
XM_017011106.2:c.4437G=	XP_016866595.1:p.Trp1479=
XM_017011107.2:c.4416G=	XP_016866596.1:p.Trp1472=
XR_002956289.1:n.4711G=
NM_001363725.2:c.2265G=	NP_001350654.1:p.Trp755=
NM_001371656.1:c.4644G=	NP_001358585.1:p.Trp1548=
NM_001374820.1:c.4644G=	NP_001361749.1:p.Trp1548=
NM_001374828.1:c.4764G= MANE Select	NP_001361757.1:p.Trp1588=
NM_017519.3:c.4605G=	NP_059989.3:p.Trp1535=