Canonical Allele Identifier: CA1675543166

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200955C= , CM000668.2:g.157200955C=	GRCh38
NC_000006.11:g.157522089C= , CM000668.1:g.157522089C=	GRCh37
NC_000006.10:g.157563781C=	NCBI36
NG_032093.1:g.428026C=
NG_032093.2:g.428026C=
NG_066624.1:g.429930C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4571C=	ENSP00000055163.8:p.Ser1524=
ENST00000414678.8:c.4640C=	ENSP00000412835.3:p.Ser1547=
ENST00000637015.2:c.4859C=	ENSP00000489729.2:p.Ser1620=
ENST00000346085.10:c.4610C=	ENSP00000344546.5:p.Ser1537=
ENST00000350026.10:c.4322C=	ENSP00000055163.7:p.Ser1441=
ENST00000414678.7:c.2888C=	ENSP00000412835.2:p.Ser963=
ENST00000635849.1:c.2051C=	ENSP00000490948.1:p.Ser684=
ENST00000635957.1:c.1682C=	ENSP00000490385.1:p.Ser561=
ENST00000636227.1:n.3193C=
ENST00000636254.1:n.650C=
ENST00000636930.2:c.4730C= MANE Select	ENSP00000490491.2:p.Ser1577=
ENST00000636940.1:n.2727C=
ENST00000637015.1:c.2098C=
ENST00000637568.1:c.2012C=
ENST00000637741.1:n.1396C=
ENST00000637810.1:c.2072C=	ENSP00000489636.1:p.Ser691=
ENST00000637904.1:c.2231C=	ENSP00000490550.1:p.Ser744=
ENST00000647938.1:c.4361C=	ENSP00000498155.1:p.Ser1454=
ENST00000346085.9:c.4361C=	ENSP00000344546.4:p.Ser1454=
ENST00000350026.9:c.4322C=	ENSP00000055163.7:p.Ser1441=
ENST00000414678.6:c.2888C=	ENSP00000412835.2:p.Ser963=
NM_017519.2:c.4322C=	NP_059989.2:p.Ser1441=
NM_020732.3:c.4361C=	NP_065783.3:p.Ser1454=
XM_005267069.3:c.4481C=	XP_005267126.2:p.Ser1494=
XM_011535984.1:c.3560C=	XP_011534286.1:p.Ser1187=
XM_011535985.1:c.3380C=	XP_011534287.1:p.Ser1127=
XM_011535986.1:c.3140C=	XP_011534288.1:p.Ser1047=
XM_011535987.1:c.2759C=	XP_011534289.1:p.Ser920=
XM_011535988.1:c.1622C=	XP_011534290.1:p.Ser541=
NM_001346813.1:c.4481C=	NP_001333742.1:p.Ser1494=
NM_001363725.1:c.2231C=	NP_001350654.1:p.Ser744=
XM_011535984.2:c.4691C=	XP_011534286.2:p.Ser1564=
XM_011535988.3:c.1622C=	XP_011534290.1:p.Ser541=
XM_017011103.2:c.4592C=	XP_016866592.1:p.Ser1531=
XM_017011104.1:c.4562C=	XP_016866593.1:p.Ser1521=
XM_017011105.2:c.4532C=	XP_016866594.1:p.Ser1511=
XM_017011106.2:c.4403C=	XP_016866595.1:p.Ser1468=
XM_017011107.2:c.4382C=	XP_016866596.1:p.Ser1461=
XR_002956289.1:n.4677C=
NM_001363725.2:c.2231C=	NP_001350654.1:p.Ser744=
NM_001371656.1:c.4610C=	NP_001358585.1:p.Ser1537=
NM_001374820.1:c.4610C=	NP_001361749.1:p.Ser1537=
NM_001374828.1:c.4730C= MANE Select	NP_001361757.1:p.Ser1577=
NM_017519.3:c.4571C=	NP_059989.3:p.Ser1524=