Canonical Allele Identifier: CA1675543173

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200964G= , CM000668.2:g.157200964G=	GRCh38
NC_000006.11:g.157522098G= , CM000668.1:g.157522098G=	GRCh37
NC_000006.10:g.157563790G=	NCBI36
NG_032093.1:g.428035G=
NG_032093.2:g.428035G=
NG_066624.1:g.429939G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4580G=	ENSP00000055163.8:p.Ser1527=
ENST00000414678.8:c.4649G=	ENSP00000412835.3:p.Ser1550=
ENST00000637015.2:c.4868G=	ENSP00000489729.2:p.Ser1623=
ENST00000346085.10:c.4619G=	ENSP00000344546.5:p.Ser1540=
ENST00000350026.10:c.4331G=	ENSP00000055163.7:p.Ser1444=
ENST00000414678.7:c.2897G=	ENSP00000412835.2:p.Ser966=
ENST00000635849.1:c.2060G=	ENSP00000490948.1:p.Ser687=
ENST00000635957.1:c.1691G=	ENSP00000490385.1:p.Ser564=
ENST00000636227.1:n.3202G=
ENST00000636254.1:n.659G=
ENST00000636930.2:c.4739G= MANE Select	ENSP00000490491.2:p.Ser1580=
ENST00000636940.1:n.2736G=
ENST00000637015.1:c.2107G=
ENST00000637568.1:c.2021G=
ENST00000637741.1:n.1405G=
ENST00000637810.1:c.2081G=	ENSP00000489636.1:p.Ser694=
ENST00000637904.1:c.2240G=	ENSP00000490550.1:p.Ser747=
ENST00000647938.1:c.4370G=	ENSP00000498155.1:p.Ser1457=
ENST00000346085.9:c.4370G=	ENSP00000344546.4:p.Ser1457=
ENST00000350026.9:c.4331G=	ENSP00000055163.7:p.Ser1444=
ENST00000414678.6:c.2897G=	ENSP00000412835.2:p.Ser966=
NM_017519.2:c.4331G=	NP_059989.2:p.Ser1444=
NM_020732.3:c.4370G=	NP_065783.3:p.Ser1457=
XM_005267069.3:c.4490G=	XP_005267126.2:p.Ser1497=
XM_011535984.1:c.3569G=	XP_011534286.1:p.Ser1190=
XM_011535985.1:c.3389G=	XP_011534287.1:p.Ser1130=
XM_011535986.1:c.3149G=	XP_011534288.1:p.Ser1050=
XM_011535987.1:c.2768G=	XP_011534289.1:p.Ser923=
XM_011535988.1:c.1631G=	XP_011534290.1:p.Ser544=
NM_001346813.1:c.4490G=	NP_001333742.1:p.Ser1497=
NM_001363725.1:c.2240G=	NP_001350654.1:p.Ser747=
XM_011535984.2:c.4700G=	XP_011534286.2:p.Ser1567=
XM_011535988.3:c.1631G=	XP_011534290.1:p.Ser544=
XM_017011103.2:c.4601G=	XP_016866592.1:p.Ser1534=
XM_017011104.1:c.4571G=	XP_016866593.1:p.Ser1524=
XM_017011105.2:c.4541G=	XP_016866594.1:p.Ser1514=
XM_017011106.2:c.4412G=	XP_016866595.1:p.Ser1471=
XM_017011107.2:c.4391G=	XP_016866596.1:p.Ser1464=
XR_002956289.1:n.4686G=
NM_001363725.2:c.2240G=	NP_001350654.1:p.Ser747=
NM_001371656.1:c.4619G=	NP_001358585.1:p.Ser1540=
NM_001374820.1:c.4619G=	NP_001361749.1:p.Ser1540=
NM_001374828.1:c.4739G= MANE Select	NP_001361757.1:p.Ser1580=
NM_017519.3:c.4580G=	NP_059989.3:p.Ser1527=