Canonical Allele Identifier: CA1675523542

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201393C= , CM000668.2:g.157201393C=	GRCh38
NC_000006.11:g.157522527C= , CM000668.1:g.157522527C=	GRCh37
NC_000006.10:g.157564219C=	NCBI36
NG_032093.1:g.428464C=
NG_032093.2:g.428464C=
NG_066624.1:g.430368C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5009C=	ENSP00000055163.8:p.Pro1670=
ENST00000414678.8:c.5078C=	ENSP00000412835.3:p.Pro1693=
ENST00000637015.2:c.5297C=	ENSP00000489729.2:p.Pro1766=
ENST00000346085.10:c.5048C=	ENSP00000344546.5:p.Pro1683=
ENST00000350026.10:c.4760C=	ENSP00000055163.7:p.Pro1587=
ENST00000414678.7:c.3326C=	ENSP00000412835.2:p.Pro1109=
ENST00000635849.1:c.2489C=	ENSP00000490948.1:p.Pro830=
ENST00000635957.1:c.2120C=	ENSP00000490385.1:p.Pro707=
ENST00000636227.1:n.3631C=
ENST00000636254.1:n.1088C=
ENST00000636930.2:c.5168C= MANE Select	ENSP00000490491.2:p.Pro1723=
ENST00000636940.1:n.3165C=
ENST00000637015.1:c.2536C=
ENST00000637568.1:c.2450C=
ENST00000637741.1:n.1834C=
ENST00000637810.1:c.2510C=	ENSP00000489636.1:p.Pro837=
ENST00000637904.1:c.2669C=	ENSP00000490550.1:p.Pro890=
ENST00000647938.1:c.4799C=	ENSP00000498155.1:p.Pro1600=
ENST00000346085.9:c.4799C=	ENSP00000344546.4:p.Pro1600=
ENST00000350026.9:c.4760C=	ENSP00000055163.7:p.Pro1587=
ENST00000414678.6:c.3326C=	ENSP00000412835.2:p.Pro1109=
NM_017519.2:c.4760C=	NP_059989.2:p.Pro1587=
NM_020732.3:c.4799C=	NP_065783.3:p.Pro1600=
XM_005267069.3:c.4919C=	XP_005267126.2:p.Pro1640=
XM_011535984.1:c.3998C=	XP_011534286.1:p.Pro1333=
XM_011535985.1:c.3818C=	XP_011534287.1:p.Pro1273=
XM_011535986.1:c.3578C=	XP_011534288.1:p.Pro1193=
XM_011535987.1:c.3197C=	XP_011534289.1:p.Pro1066=
XM_011535988.1:c.2060C=	XP_011534290.1:p.Pro687=
NM_001346813.1:c.4919C=	NP_001333742.1:p.Pro1640=
NM_001363725.1:c.2669C=	NP_001350654.1:p.Pro890=
XM_011535984.2:c.5129C=	XP_011534286.2:p.Pro1710=
XM_011535988.3:c.2060C=	XP_011534290.1:p.Pro687=
XM_017011103.2:c.5030C=	XP_016866592.1:p.Pro1677=
XM_017011104.1:c.5000C=	XP_016866593.1:p.Pro1667=
XM_017011105.2:c.4970C=	XP_016866594.1:p.Pro1657=
XM_017011106.2:c.4841C=	XP_016866595.1:p.Pro1614=
XM_017011107.2:c.4820C=	XP_016866596.1:p.Pro1607=
XR_002956289.1:n.5115C=
NM_001363725.2:c.2669C=	NP_001350654.1:p.Pro890=
NM_001371656.1:c.5048C=	NP_001358585.1:p.Pro1683=
NM_001374820.1:c.5048C=	NP_001361749.1:p.Pro1683=
NM_001374828.1:c.5168C= MANE Select	NP_001361757.1:p.Pro1723=
NM_017519.3:c.5009C=	NP_059989.3:p.Pro1670=