Canonical Allele Identifier: CA3135089315

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200867T= , CM000668.2:g.157200867T=	GRCh38
NC_000006.11:g.157522001T= , CM000668.1:g.157522001T=	GRCh37
NC_000006.10:g.157563693T=	NCBI36
NG_032093.1:g.427938T=
NG_032093.2:g.427938T=
NG_066624.1:g.429842T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4642T= MANE Select	NP_001361757.1:p.Tyr1548=
ENST00000636930.2:c.4642T= MANE Select	ENSP00000490491.2:p.Tyr1548=
NM_001346813.1:c.4393T=	NP_001333742.1:p.Tyr1465=
NM_001363725.1:c.2143T=	NP_001350654.1:p.Tyr715=
NM_001363725.2:c.2143T=	NP_001350654.1:p.Tyr715=
NM_001371656.1:c.4522T=	NP_001358585.1:p.Tyr1508=
NM_001374820.1:c.4522T=	NP_001361749.1:p.Tyr1508=
NM_017519.2:c.4234T=	NP_059989.2:p.Tyr1412=
NM_017519.3:c.4483T=	NP_059989.3:p.Tyr1495=
NM_020732.3:c.4273T=	NP_065783.3:p.Tyr1425=
ENST00000346085.10:c.4522T=	ENSP00000344546.5:p.Tyr1508=
ENST00000346085.9:c.4273T=	ENSP00000344546.4:p.Tyr1425=
ENST00000350026.10:c.4234T=	ENSP00000055163.7:p.Tyr1412=
ENST00000350026.11:c.4483T=	ENSP00000055163.8:p.Tyr1495=
ENST00000350026.9:c.4234T=	ENSP00000055163.7:p.Tyr1412=
ENST00000414678.6:c.2800T=	ENSP00000412835.2:p.Tyr934=
ENST00000414678.7:c.2800T=	ENSP00000412835.2:p.Tyr934=
ENST00000414678.8:c.4552T=	ENSP00000412835.3:p.Tyr1518=
ENST00000635849.1:c.1963T=	ENSP00000490948.1:p.Tyr655=
ENST00000635957.1:c.1594T=	ENSP00000490385.1:p.Tyr532=
ENST00000636227.1:n.3105T=
ENST00000636254.1:n.562T=
ENST00000636940.1:n.2639T=
ENST00000637015.1:c.2010T=
ENST00000637015.2:c.4771T=	ENSP00000489729.2:p.Tyr1591=
ENST00000637568.1:c.1924T=
ENST00000637741.1:n.1308T=
ENST00000637810.1:c.1984T=	ENSP00000489636.1:p.Tyr662=
ENST00000637904.1:c.2143T=	ENSP00000490550.1:p.Tyr715=
ENST00000647938.1:c.4273T=	ENSP00000498155.1:p.Tyr1425=
XM_005267069.3:c.4393T=	XP_005267126.2:p.Tyr1465=
XM_011535984.1:c.3472T=	XP_011534286.1:p.Tyr1158=
XM_011535984.2:c.4603T=	XP_011534286.2:p.Tyr1535=
XM_011535985.1:c.3292T=	XP_011534287.1:p.Tyr1098=
XM_011535986.1:c.3052T=	XP_011534288.1:p.Tyr1018=
XM_011535987.1:c.2671T=	XP_011534289.1:p.Tyr891=
XM_011535988.1:c.1534T=	XP_011534290.1:p.Tyr512=
XM_011535988.3:c.1534T=	XP_011534290.1:p.Tyr512=
XM_017011103.2:c.4504T=	XP_016866592.1:p.Tyr1502=
XM_017011104.1:c.4474T=	XP_016866593.1:p.Tyr1492=
XM_017011105.2:c.4444T=	XP_016866594.1:p.Tyr1482=
XM_017011106.2:c.4315T=	XP_016866595.1:p.Tyr1439=
XM_017011107.2:c.4294T=	XP_016866596.1:p.Tyr1432=
XR_002956289.1:n.4589T=