Canonical Allele Identifier: CA1675522860

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201041G= , CM000668.2:g.157201041G=	GRCh38
NC_000006.11:g.157522175G= , CM000668.1:g.157522175G=	GRCh37
NC_000006.10:g.157563867G=	NCBI36
NG_032093.1:g.428112G=
NG_032093.2:g.428112G=
NG_066624.1:g.430016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4657G=	ENSP00000055163.8:p.Gly1553=
ENST00000414678.8:c.4726G=	ENSP00000412835.3:p.Gly1576=
ENST00000637015.2:c.4945G=	ENSP00000489729.2:p.Gly1649=
ENST00000346085.10:c.4696G=	ENSP00000344546.5:p.Gly1566=
ENST00000350026.10:c.4408G=	ENSP00000055163.7:p.Gly1470=
ENST00000414678.7:c.2974G=	ENSP00000412835.2:p.Gly992=
ENST00000635849.1:c.2137G=	ENSP00000490948.1:p.Gly713=
ENST00000635957.1:c.1768G=	ENSP00000490385.1:p.Gly590=
ENST00000636227.1:n.3279G=
ENST00000636254.1:n.736G=
ENST00000636930.2:c.4816G= MANE Select	ENSP00000490491.2:p.Gly1606=
ENST00000636940.1:n.2813G=
ENST00000637015.1:c.2184G=
ENST00000637568.1:c.2098G=
ENST00000637741.1:n.1482G=
ENST00000637810.1:c.2158G=	ENSP00000489636.1:p.Gly720=
ENST00000637904.1:c.2317G=	ENSP00000490550.1:p.Gly773=
ENST00000647938.1:c.4447G=	ENSP00000498155.1:p.Gly1483=
ENST00000346085.9:c.4447G=	ENSP00000344546.4:p.Gly1483=
ENST00000350026.9:c.4408G=	ENSP00000055163.7:p.Gly1470=
ENST00000414678.6:c.2974G=	ENSP00000412835.2:p.Gly992=
NM_017519.2:c.4408G=	NP_059989.2:p.Gly1470=
NM_020732.3:c.4447G=	NP_065783.3:p.Gly1483=
XM_005267069.3:c.4567G=	XP_005267126.2:p.Gly1523=
XM_011535984.1:c.3646G=	XP_011534286.1:p.Gly1216=
XM_011535985.1:c.3466G=	XP_011534287.1:p.Gly1156=
XM_011535986.1:c.3226G=	XP_011534288.1:p.Gly1076=
XM_011535987.1:c.2845G=	XP_011534289.1:p.Gly949=
XM_011535988.1:c.1708G=	XP_011534290.1:p.Gly570=
NM_001346813.1:c.4567G=	NP_001333742.1:p.Gly1523=
NM_001363725.1:c.2317G=	NP_001350654.1:p.Gly773=
XM_011535984.2:c.4777G=	XP_011534286.2:p.Gly1593=
XM_011535988.3:c.1708G=	XP_011534290.1:p.Gly570=
XM_017011103.2:c.4678G=	XP_016866592.1:p.Gly1560=
XM_017011104.1:c.4648G=	XP_016866593.1:p.Gly1550=
XM_017011105.2:c.4618G=	XP_016866594.1:p.Gly1540=
XM_017011106.2:c.4489G=	XP_016866595.1:p.Gly1497=
XM_017011107.2:c.4468G=	XP_016866596.1:p.Gly1490=
XR_002956289.1:n.4763G=
NM_001363725.2:c.2317G=	NP_001350654.1:p.Gly773=
NM_001371656.1:c.4696G=	NP_001358585.1:p.Gly1566=
NM_001374820.1:c.4696G=	NP_001361749.1:p.Gly1566=
NM_001374828.1:c.4816G= MANE Select	NP_001361757.1:p.Gly1606=
NM_017519.3:c.4657G=	NP_059989.3:p.Gly1553=