Canonical Allele Identifier: CA1675522974

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201096T= , CM000668.2:g.157201096T=	GRCh38
NC_000006.11:g.157522230T= , CM000668.1:g.157522230T=	GRCh37
NC_000006.10:g.157563922T=	NCBI36
NG_032093.1:g.428167T=
NG_032093.2:g.428167T=
NG_066624.1:g.430071T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4712T=	ENSP00000055163.8:p.Val1571=
ENST00000414678.8:c.4781T=	ENSP00000412835.3:p.Val1594=
ENST00000637015.2:c.5000T=	ENSP00000489729.2:p.Val1667=
ENST00000346085.10:c.4751T=	ENSP00000344546.5:p.Val1584=
ENST00000350026.10:c.4463T=	ENSP00000055163.7:p.Val1488=
ENST00000414678.7:c.3029T=	ENSP00000412835.2:p.Val1010=
ENST00000635849.1:c.2192T=	ENSP00000490948.1:p.Val731=
ENST00000635957.1:c.1823T=	ENSP00000490385.1:p.Val608=
ENST00000636227.1:n.3334T=
ENST00000636254.1:n.791T=
ENST00000636930.2:c.4871T= MANE Select	ENSP00000490491.2:p.Val1624=
ENST00000636940.1:n.2868T=
ENST00000637015.1:c.2239T=
ENST00000637568.1:c.2153T=
ENST00000637741.1:n.1537T=
ENST00000637810.1:c.2213T=	ENSP00000489636.1:p.Val738=
ENST00000637904.1:c.2372T=	ENSP00000490550.1:p.Val791=
ENST00000647938.1:c.4502T=	ENSP00000498155.1:p.Val1501=
ENST00000346085.9:c.4502T=	ENSP00000344546.4:p.Val1501=
ENST00000350026.9:c.4463T=	ENSP00000055163.7:p.Val1488=
ENST00000414678.6:c.3029T=	ENSP00000412835.2:p.Val1010=
NM_017519.2:c.4463T=	NP_059989.2:p.Val1488=
NM_020732.3:c.4502T=	NP_065783.3:p.Val1501=
XM_005267069.3:c.4622T=	XP_005267126.2:p.Val1541=
XM_011535984.1:c.3701T=	XP_011534286.1:p.Val1234=
XM_011535985.1:c.3521T=	XP_011534287.1:p.Val1174=
XM_011535986.1:c.3281T=	XP_011534288.1:p.Val1094=
XM_011535987.1:c.2900T=	XP_011534289.1:p.Val967=
XM_011535988.1:c.1763T=	XP_011534290.1:p.Val588=
NM_001346813.1:c.4622T=	NP_001333742.1:p.Val1541=
NM_001363725.1:c.2372T=	NP_001350654.1:p.Val791=
XM_011535984.2:c.4832T=	XP_011534286.2:p.Val1611=
XM_011535988.3:c.1763T=	XP_011534290.1:p.Val588=
XM_017011103.2:c.4733T=	XP_016866592.1:p.Val1578=
XM_017011104.1:c.4703T=	XP_016866593.1:p.Val1568=
XM_017011105.2:c.4673T=	XP_016866594.1:p.Val1558=
XM_017011106.2:c.4544T=	XP_016866595.1:p.Val1515=
XM_017011107.2:c.4523T=	XP_016866596.1:p.Val1508=
XR_002956289.1:n.4818T=
NM_001363725.2:c.2372T=	NP_001350654.1:p.Val791=
NM_001371656.1:c.4751T=	NP_001358585.1:p.Val1584=
NM_001374820.1:c.4751T=	NP_001361749.1:p.Val1584=
NM_001374828.1:c.4871T= MANE Select	NP_001361757.1:p.Val1624=
NM_017519.3:c.4712T=	NP_059989.3:p.Val1571=