Canonical Allele Identifier: CA1675538226

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189655C= , CM000668.2:g.157189655C=	GRCh38
NC_000006.11:g.157510789C= , CM000668.1:g.157510789C=	GRCh37
NC_000006.10:g.157552481C=	NCBI36
NG_032093.1:g.416726C=
NG_032093.2:g.416726C=
NG_066624.1:g.418630C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3774C=	ENSP00000055163.8:p.Ser1258=
ENST00000414678.8:c.3843C=	ENSP00000412835.3:p.Ser1281=
ENST00000637015.2:c.4062C=	ENSP00000489729.2:p.Ser1354=
ENST00000346085.10:c.3813C=	ENSP00000344546.5:p.Ser1271=
ENST00000350026.10:c.3525C=	ENSP00000055163.7:p.Ser1175=
ENST00000414678.7:c.2091C=	ENSP00000412835.2:p.Ser697=
ENST00000635849.1:c.1254C=	ENSP00000490948.1:p.Ser418=
ENST00000635957.1:c.888C=	ENSP00000490385.1:p.Ser296=
ENST00000636930.2:c.3933C= MANE Select	ENSP00000490491.2:p.Ser1311=
ENST00000636940.1:n.1930C=
ENST00000637015.1:c.1301C=
ENST00000637568.1:c.1215C=
ENST00000637741.1:n.599C=
ENST00000637810.1:c.1275C=	ENSP00000489636.1:p.Ser425=
ENST00000637904.1:c.1434C=	ENSP00000490550.1:p.Ser478=
ENST00000647938.1:c.3564C=	ENSP00000498155.1:p.Ser1188=
ENST00000346085.9:c.3564C=	ENSP00000344546.4:p.Ser1188=
ENST00000350026.9:c.3525C=	ENSP00000055163.7:p.Ser1175=
ENST00000414678.6:c.2091C=	ENSP00000412835.2:p.Ser697=
NM_017519.2:c.3525C=	NP_059989.2:p.Ser1175=
NM_020732.3:c.3564C=	NP_065783.3:p.Ser1188=
XM_005267069.3:c.3684C=	XP_005267126.2:p.Ser1228=
XM_011535984.1:c.2763C=	XP_011534286.1:p.Ser921=
XM_011535985.1:c.2583C=	XP_011534287.1:p.Ser861=
XM_011535986.1:c.2343C=	XP_011534288.1:p.Ser781=
XM_011535987.1:c.1962C=	XP_011534289.1:p.Ser654=
XM_011535988.1:c.825C=	XP_011534290.1:p.Ser275=
NM_001346813.1:c.3684C=	NP_001333742.1:p.Ser1228=
NM_001363725.1:c.1434C=	NP_001350654.1:p.Ser478=
XM_011535984.2:c.3894C=	XP_011534286.2:p.Ser1298=
XM_011535988.3:c.825C=	XP_011534290.1:p.Ser275=
XM_017011103.2:c.3795C=	XP_016866592.1:p.Ser1265=
XM_017011104.1:c.3765C=	XP_016866593.1:p.Ser1255=
XM_017011105.2:c.3735C=	XP_016866594.1:p.Ser1245=
XM_017011106.2:c.3606C=	XP_016866595.1:p.Ser1202=
XM_017011107.2:c.3585C=	XP_016866596.1:p.Ser1195=
XR_002956289.1:n.3977C=
NM_001363725.2:c.1434C=	NP_001350654.1:p.Ser478=
NM_001371656.1:c.3813C=	NP_001358585.1:p.Ser1271=
NM_001374820.1:c.3813C=	NP_001361749.1:p.Ser1271=
NM_001374828.1:c.3933C= MANE Select	NP_001361757.1:p.Ser1311=
NM_017519.3:c.3774C=	NP_059989.3:p.Ser1258=