Canonical Allele Identifier: CA1675538239

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189681C= , CM000668.2:g.157189681C=	GRCh38
NC_000006.11:g.157510815C= , CM000668.1:g.157510815C=	GRCh37
NC_000006.10:g.157552507C=	NCBI36
NG_032093.1:g.416752C=
NG_032093.2:g.416752C=
NG_066624.1:g.418656C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3800C=	ENSP00000055163.8:p.Ser1267=
ENST00000414678.8:c.3869C=	ENSP00000412835.3:p.Ser1290=
ENST00000637015.2:c.4088C=	ENSP00000489729.2:p.Ser1363=
ENST00000346085.10:c.3839C=	ENSP00000344546.5:p.Ser1280=
ENST00000350026.10:c.3551C=	ENSP00000055163.7:p.Ser1184=
ENST00000414678.7:c.2117C=	ENSP00000412835.2:p.Ser706=
ENST00000635849.1:c.1280C=	ENSP00000490948.1:p.Ser427=
ENST00000635957.1:c.914C=	ENSP00000490385.1:p.Ser305=
ENST00000636930.2:c.3959C= MANE Select	ENSP00000490491.2:p.Ser1320=
ENST00000636940.1:n.1956C=
ENST00000637015.1:c.1327C=
ENST00000637568.1:c.1241C=
ENST00000637741.1:n.625C=
ENST00000637810.1:c.1301C=	ENSP00000489636.1:p.Ser434=
ENST00000637904.1:c.1460C=	ENSP00000490550.1:p.Ser487=
ENST00000647938.1:c.3590C=	ENSP00000498155.1:p.Ser1197=
ENST00000346085.9:c.3590C=	ENSP00000344546.4:p.Ser1197=
ENST00000350026.9:c.3551C=	ENSP00000055163.7:p.Ser1184=
ENST00000414678.6:c.2117C=	ENSP00000412835.2:p.Ser706=
NM_017519.2:c.3551C=	NP_059989.2:p.Ser1184=
NM_020732.3:c.3590C=	NP_065783.3:p.Ser1197=
XM_005267069.3:c.3710C=	XP_005267126.2:p.Ser1237=
XM_011535984.1:c.2789C=	XP_011534286.1:p.Ser930=
XM_011535985.1:c.2609C=	XP_011534287.1:p.Ser870=
XM_011535986.1:c.2369C=	XP_011534288.1:p.Ser790=
XM_011535987.1:c.1988C=	XP_011534289.1:p.Ser663=
XM_011535988.1:c.851C=	XP_011534290.1:p.Ser284=
NM_001346813.1:c.3710C=	NP_001333742.1:p.Ser1237=
NM_001363725.1:c.1460C=	NP_001350654.1:p.Ser487=
XM_011535984.2:c.3920C=	XP_011534286.2:p.Ser1307=
XM_011535988.3:c.851C=	XP_011534290.1:p.Ser284=
XM_017011103.2:c.3821C=	XP_016866592.1:p.Ser1274=
XM_017011104.1:c.3791C=	XP_016866593.1:p.Ser1264=
XM_017011105.2:c.3761C=	XP_016866594.1:p.Ser1254=
XM_017011106.2:c.3632C=	XP_016866595.1:p.Ser1211=
XM_017011107.2:c.3611C=	XP_016866596.1:p.Ser1204=
XR_002956289.1:n.4003C=
NM_001363725.2:c.1460C=	NP_001350654.1:p.Ser487=
NM_001371656.1:c.3839C=	NP_001358585.1:p.Ser1280=
NM_001374820.1:c.3839C=	NP_001361749.1:p.Ser1280=
NM_001374828.1:c.3959C= MANE Select	NP_001361757.1:p.Ser1320=
NM_017519.3:c.3800C=	NP_059989.3:p.Ser1267=