Canonical Allele Identifier: CA1675523154

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201208G= , CM000668.2:g.157201208G=	GRCh38
NC_000006.11:g.157522342G= , CM000668.1:g.157522342G=	GRCh37
NC_000006.10:g.157564034G=	NCBI36
NG_032093.1:g.428279G=
NG_032093.2:g.428279G=
NG_066624.1:g.430183G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4824G=	ENSP00000055163.8:p.Pro1608=
ENST00000414678.8:c.4893G=	ENSP00000412835.3:p.Pro1631=
ENST00000637015.2:c.5112G=	ENSP00000489729.2:p.Pro1704=
ENST00000346085.10:c.4863G=	ENSP00000344546.5:p.Pro1621=
ENST00000350026.10:c.4575G=	ENSP00000055163.7:p.Pro1525=
ENST00000414678.7:c.3141G=	ENSP00000412835.2:p.Pro1047=
ENST00000635849.1:c.2304G=	ENSP00000490948.1:p.Pro768=
ENST00000635957.1:c.1935G=	ENSP00000490385.1:p.Pro645=
ENST00000636227.1:n.3446G=
ENST00000636254.1:n.903G=
ENST00000636930.2:c.4983G= MANE Select	ENSP00000490491.2:p.Pro1661=
ENST00000636940.1:n.2980G=
ENST00000637015.1:c.2351G=
ENST00000637568.1:c.2265G=
ENST00000637741.1:n.1649G=
ENST00000637810.1:c.2325G=	ENSP00000489636.1:p.Pro775=
ENST00000637904.1:c.2484G=	ENSP00000490550.1:p.Pro828=
ENST00000647938.1:c.4614G=	ENSP00000498155.1:p.Pro1538=
ENST00000346085.9:c.4614G=	ENSP00000344546.4:p.Pro1538=
ENST00000350026.9:c.4575G=	ENSP00000055163.7:p.Pro1525=
ENST00000414678.6:c.3141G=	ENSP00000412835.2:p.Pro1047=
NM_017519.2:c.4575G=	NP_059989.2:p.Pro1525=
NM_020732.3:c.4614G=	NP_065783.3:p.Pro1538=
XM_005267069.3:c.4734G=	XP_005267126.2:p.Pro1578=
XM_011535984.1:c.3813G=	XP_011534286.1:p.Pro1271=
XM_011535985.1:c.3633G=	XP_011534287.1:p.Pro1211=
XM_011535986.1:c.3393G=	XP_011534288.1:p.Pro1131=
XM_011535987.1:c.3012G=	XP_011534289.1:p.Pro1004=
XM_011535988.1:c.1875G=	XP_011534290.1:p.Pro625=
NM_001346813.1:c.4734G=	NP_001333742.1:p.Pro1578=
NM_001363725.1:c.2484G=	NP_001350654.1:p.Pro828=
XM_011535984.2:c.4944G=	XP_011534286.2:p.Pro1648=
XM_011535988.3:c.1875G=	XP_011534290.1:p.Pro625=
XM_017011103.2:c.4845G=	XP_016866592.1:p.Pro1615=
XM_017011104.1:c.4815G=	XP_016866593.1:p.Pro1605=
XM_017011105.2:c.4785G=	XP_016866594.1:p.Pro1595=
XM_017011106.2:c.4656G=	XP_016866595.1:p.Pro1552=
XM_017011107.2:c.4635G=	XP_016866596.1:p.Pro1545=
XR_002956289.1:n.4930G=
NM_001363725.2:c.2484G=	NP_001350654.1:p.Pro828=
NM_001371656.1:c.4863G=	NP_001358585.1:p.Pro1621=
NM_001374820.1:c.4863G=	NP_001361749.1:p.Pro1621=
NM_001374828.1:c.4983G= MANE Select	NP_001361757.1:p.Pro1661=
NM_017519.3:c.4824G=	NP_059989.3:p.Pro1608=