Canonical Allele Identifier: CA1675522920

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201066C= , CM000668.2:g.157201066C=	GRCh38
NC_000006.11:g.157522200C= , CM000668.1:g.157522200C=	GRCh37
NC_000006.10:g.157563892C=	NCBI36
NG_032093.1:g.428137C=
NG_032093.2:g.428137C=
NG_066624.1:g.430041C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4682C=	ENSP00000055163.8:p.Pro1561=
ENST00000414678.8:c.4751C=	ENSP00000412835.3:p.Pro1584=
ENST00000637015.2:c.4970C=	ENSP00000489729.2:p.Pro1657=
ENST00000346085.10:c.4721C=	ENSP00000344546.5:p.Pro1574=
ENST00000350026.10:c.4433C=	ENSP00000055163.7:p.Pro1478=
ENST00000414678.7:c.2999C=	ENSP00000412835.2:p.Pro1000=
ENST00000635849.1:c.2162C=	ENSP00000490948.1:p.Pro721=
ENST00000635957.1:c.1793C=	ENSP00000490385.1:p.Pro598=
ENST00000636227.1:n.3304C=
ENST00000636254.1:n.761C=
ENST00000636930.2:c.4841C= MANE Select	ENSP00000490491.2:p.Pro1614=
ENST00000636940.1:n.2838C=
ENST00000637015.1:c.2209C=
ENST00000637568.1:c.2123C=
ENST00000637741.1:n.1507C=
ENST00000637810.1:c.2183C=	ENSP00000489636.1:p.Pro728=
ENST00000637904.1:c.2342C=	ENSP00000490550.1:p.Pro781=
ENST00000647938.1:c.4472C=	ENSP00000498155.1:p.Pro1491=
ENST00000346085.9:c.4472C=	ENSP00000344546.4:p.Pro1491=
ENST00000350026.9:c.4433C=	ENSP00000055163.7:p.Pro1478=
ENST00000414678.6:c.2999C=	ENSP00000412835.2:p.Pro1000=
NM_017519.2:c.4433C=	NP_059989.2:p.Pro1478=
NM_020732.3:c.4472C=	NP_065783.3:p.Pro1491=
XM_005267069.3:c.4592C=	XP_005267126.2:p.Pro1531=
XM_011535984.1:c.3671C=	XP_011534286.1:p.Pro1224=
XM_011535985.1:c.3491C=	XP_011534287.1:p.Pro1164=
XM_011535986.1:c.3251C=	XP_011534288.1:p.Pro1084=
XM_011535987.1:c.2870C=	XP_011534289.1:p.Pro957=
XM_011535988.1:c.1733C=	XP_011534290.1:p.Pro578=
NM_001346813.1:c.4592C=	NP_001333742.1:p.Pro1531=
NM_001363725.1:c.2342C=	NP_001350654.1:p.Pro781=
XM_011535984.2:c.4802C=	XP_011534286.2:p.Pro1601=
XM_011535988.3:c.1733C=	XP_011534290.1:p.Pro578=
XM_017011103.2:c.4703C=	XP_016866592.1:p.Pro1568=
XM_017011104.1:c.4673C=	XP_016866593.1:p.Pro1558=
XM_017011105.2:c.4643C=	XP_016866594.1:p.Pro1548=
XM_017011106.2:c.4514C=	XP_016866595.1:p.Pro1505=
XM_017011107.2:c.4493C=	XP_016866596.1:p.Pro1498=
XR_002956289.1:n.4788C=
NM_001363725.2:c.2342C=	NP_001350654.1:p.Pro781=
NM_001371656.1:c.4721C=	NP_001358585.1:p.Pro1574=
NM_001374820.1:c.4721C=	NP_001361749.1:p.Pro1574=
NM_001374828.1:c.4841C= MANE Select	NP_001361757.1:p.Pro1614=
NM_017519.3:c.4682C=	NP_059989.3:p.Pro1561=