Canonical Allele Identifier: CA1675538260

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189734C= , CM000668.2:g.157189734C=	GRCh38
NC_000006.11:g.157510868C= , CM000668.1:g.157510868C=	GRCh37
NC_000006.10:g.157552560C=	NCBI36
NG_032093.1:g.416805C=
NG_032093.2:g.416805C=
NG_066624.1:g.418709C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3853C=	ENSP00000055163.8:p.Pro1285=
ENST00000414678.8:c.3922C=	ENSP00000412835.3:p.Pro1308=
ENST00000637015.2:c.4141C=	ENSP00000489729.2:p.Pro1381=
ENST00000346085.10:c.3892C=	ENSP00000344546.5:p.Pro1298=
ENST00000350026.10:c.3604C=	ENSP00000055163.7:p.Pro1202=
ENST00000414678.7:c.2170C=	ENSP00000412835.2:p.Pro724=
ENST00000635849.1:c.1333C=	ENSP00000490948.1:p.Pro445=
ENST00000635957.1:c.967C=	ENSP00000490385.1:p.Pro323=
ENST00000636930.2:c.4012C= MANE Select	ENSP00000490491.2:p.Pro1338=
ENST00000636940.1:n.2009C=
ENST00000637015.1:c.1380C=
ENST00000637568.1:c.1294C=
ENST00000637741.1:n.678C=
ENST00000637810.1:c.1354C=	ENSP00000489636.1:p.Pro452=
ENST00000637904.1:c.1513C=	ENSP00000490550.1:p.Pro505=
ENST00000647938.1:c.3643C=	ENSP00000498155.1:p.Pro1215=
ENST00000346085.9:c.3643C=	ENSP00000344546.4:p.Pro1215=
ENST00000350026.9:c.3604C=	ENSP00000055163.7:p.Pro1202=
ENST00000414678.6:c.2170C=	ENSP00000412835.2:p.Pro724=
NM_017519.2:c.3604C=	NP_059989.2:p.Pro1202=
NM_020732.3:c.3643C=	NP_065783.3:p.Pro1215=
XM_005267069.3:c.3763C=	XP_005267126.2:p.Pro1255=
XM_011535984.1:c.2842C=	XP_011534286.1:p.Pro948=
XM_011535985.1:c.2662C=	XP_011534287.1:p.Pro888=
XM_011535986.1:c.2422C=	XP_011534288.1:p.Pro808=
XM_011535987.1:c.2041C=	XP_011534289.1:p.Pro681=
XM_011535988.1:c.904C=	XP_011534290.1:p.Pro302=
NM_001346813.1:c.3763C=	NP_001333742.1:p.Pro1255=
NM_001363725.1:c.1513C=	NP_001350654.1:p.Pro505=
XM_011535984.2:c.3973C=	XP_011534286.2:p.Pro1325=
XM_011535988.3:c.904C=	XP_011534290.1:p.Pro302=
XM_017011103.2:c.3874C=	XP_016866592.1:p.Pro1292=
XM_017011104.1:c.3844C=	XP_016866593.1:p.Pro1282=
XM_017011105.2:c.3814C=	XP_016866594.1:p.Pro1272=
XM_017011106.2:c.3685C=	XP_016866595.1:p.Pro1229=
XM_017011107.2:c.3664C=	XP_016866596.1:p.Pro1222=
XR_002956289.1:n.4056C=
NM_001363725.2:c.1513C=	NP_001350654.1:p.Pro505=
NM_001371656.1:c.3892C=	NP_001358585.1:p.Pro1298=
NM_001374820.1:c.3892C=	NP_001361749.1:p.Pro1298=
NM_001374828.1:c.4012C= MANE Select	NP_001361757.1:p.Pro1338=
NM_017519.3:c.3853C=	NP_059989.3:p.Pro1285=