Canonical Allele Identifier: CA1675523263

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201259C= , CM000668.2:g.157201259C=	GRCh38
NC_000006.11:g.157522393C= , CM000668.1:g.157522393C=	GRCh37
NC_000006.10:g.157564085C=	NCBI36
NG_032093.1:g.428330C=
NG_032093.2:g.428330C=
NG_066624.1:g.430234C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4875C=	ENSP00000055163.8:p.Ser1625=
ENST00000414678.8:c.4944C=	ENSP00000412835.3:p.Ser1648=
ENST00000637015.2:c.5163C=	ENSP00000489729.2:p.Ser1721=
ENST00000346085.10:c.4914C=	ENSP00000344546.5:p.Ser1638=
ENST00000350026.10:c.4626C=	ENSP00000055163.7:p.Ser1542=
ENST00000414678.7:c.3192C=	ENSP00000412835.2:p.Ser1064=
ENST00000635849.1:c.2355C=	ENSP00000490948.1:p.Ser785=
ENST00000635957.1:c.1986C=	ENSP00000490385.1:p.Ser662=
ENST00000636227.1:n.3497C=
ENST00000636254.1:n.954C=
ENST00000636930.2:c.5034C= MANE Select	ENSP00000490491.2:p.Ser1678=
ENST00000636940.1:n.3031C=
ENST00000637015.1:c.2402C=
ENST00000637568.1:c.2316C=
ENST00000637741.1:n.1700C=
ENST00000637810.1:c.2376C=	ENSP00000489636.1:p.Ser792=
ENST00000637904.1:c.2535C=	ENSP00000490550.1:p.Ser845=
ENST00000647938.1:c.4665C=	ENSP00000498155.1:p.Ser1555=
ENST00000346085.9:c.4665C=	ENSP00000344546.4:p.Ser1555=
ENST00000350026.9:c.4626C=	ENSP00000055163.7:p.Ser1542=
ENST00000414678.6:c.3192C=	ENSP00000412835.2:p.Ser1064=
NM_017519.2:c.4626C=	NP_059989.2:p.Ser1542=
NM_020732.3:c.4665C=	NP_065783.3:p.Ser1555=
XM_005267069.3:c.4785C=	XP_005267126.2:p.Ser1595=
XM_011535984.1:c.3864C=	XP_011534286.1:p.Ser1288=
XM_011535985.1:c.3684C=	XP_011534287.1:p.Ser1228=
XM_011535986.1:c.3444C=	XP_011534288.1:p.Ser1148=
XM_011535987.1:c.3063C=	XP_011534289.1:p.Ser1021=
XM_011535988.1:c.1926C=	XP_011534290.1:p.Ser642=
NM_001346813.1:c.4785C=	NP_001333742.1:p.Ser1595=
NM_001363725.1:c.2535C=	NP_001350654.1:p.Ser845=
XM_011535984.2:c.4995C=	XP_011534286.2:p.Ser1665=
XM_011535988.3:c.1926C=	XP_011534290.1:p.Ser642=
XM_017011103.2:c.4896C=	XP_016866592.1:p.Ser1632=
XM_017011104.1:c.4866C=	XP_016866593.1:p.Ser1622=
XM_017011105.2:c.4836C=	XP_016866594.1:p.Ser1612=
XM_017011106.2:c.4707C=	XP_016866595.1:p.Ser1569=
XM_017011107.2:c.4686C=	XP_016866596.1:p.Ser1562=
XR_002956289.1:n.4981C=
NM_001363725.2:c.2535C=	NP_001350654.1:p.Ser845=
NM_001371656.1:c.4914C=	NP_001358585.1:p.Ser1638=
NM_001374820.1:c.4914C=	NP_001361749.1:p.Ser1638=
NM_001374828.1:c.5034C= MANE Select	NP_001361757.1:p.Ser1678=
NM_017519.3:c.4875C=	NP_059989.3:p.Ser1625=