Canonical Allele Identifier: CA1675523043

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201134T= , CM000668.2:g.157201134T=	GRCh38
NC_000006.11:g.157522268T= , CM000668.1:g.157522268T=	GRCh37
NC_000006.10:g.157563960T=	NCBI36
NG_032093.1:g.428205T=
NG_032093.2:g.428205T=
NG_066624.1:g.430109T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4750T=	ENSP00000055163.8:p.Ser1584=
ENST00000414678.8:c.4819T=	ENSP00000412835.3:p.Ser1607=
ENST00000637015.2:c.5038T=	ENSP00000489729.2:p.Ser1680=
ENST00000346085.10:c.4789T=	ENSP00000344546.5:p.Ser1597=
ENST00000350026.10:c.4501T=	ENSP00000055163.7:p.Ser1501=
ENST00000414678.7:c.3067T=	ENSP00000412835.2:p.Ser1023=
ENST00000635849.1:c.2230T=	ENSP00000490948.1:p.Ser744=
ENST00000635957.1:c.1861T=	ENSP00000490385.1:p.Ser621=
ENST00000636227.1:n.3372T=
ENST00000636254.1:n.829T=
ENST00000636930.2:c.4909T= MANE Select	ENSP00000490491.2:p.Ser1637=
ENST00000636940.1:n.2906T=
ENST00000637015.1:c.2277T=
ENST00000637568.1:c.2191T=
ENST00000637741.1:n.1575T=
ENST00000637810.1:c.2251T=	ENSP00000489636.1:p.Ser751=
ENST00000637904.1:c.2410T=	ENSP00000490550.1:p.Ser804=
ENST00000647938.1:c.4540T=	ENSP00000498155.1:p.Ser1514=
ENST00000346085.9:c.4540T=	ENSP00000344546.4:p.Ser1514=
ENST00000350026.9:c.4501T=	ENSP00000055163.7:p.Ser1501=
ENST00000414678.6:c.3067T=	ENSP00000412835.2:p.Ser1023=
NM_017519.2:c.4501T=	NP_059989.2:p.Ser1501=
NM_020732.3:c.4540T=	NP_065783.3:p.Ser1514=
XM_005267069.3:c.4660T=	XP_005267126.2:p.Ser1554=
XM_011535984.1:c.3739T=	XP_011534286.1:p.Ser1247=
XM_011535985.1:c.3559T=	XP_011534287.1:p.Ser1187=
XM_011535986.1:c.3319T=	XP_011534288.1:p.Ser1107=
XM_011535987.1:c.2938T=	XP_011534289.1:p.Ser980=
XM_011535988.1:c.1801T=	XP_011534290.1:p.Ser601=
NM_001346813.1:c.4660T=	NP_001333742.1:p.Ser1554=
NM_001363725.1:c.2410T=	NP_001350654.1:p.Ser804=
XM_011535984.2:c.4870T=	XP_011534286.2:p.Ser1624=
XM_011535988.3:c.1801T=	XP_011534290.1:p.Ser601=
XM_017011103.2:c.4771T=	XP_016866592.1:p.Ser1591=
XM_017011104.1:c.4741T=	XP_016866593.1:p.Ser1581=
XM_017011105.2:c.4711T=	XP_016866594.1:p.Ser1571=
XM_017011106.2:c.4582T=	XP_016866595.1:p.Ser1528=
XM_017011107.2:c.4561T=	XP_016866596.1:p.Ser1521=
XR_002956289.1:n.4856T=
NM_001363725.2:c.2410T=	NP_001350654.1:p.Ser804=
NM_001371656.1:c.4789T=	NP_001358585.1:p.Ser1597=
NM_001374820.1:c.4789T=	NP_001361749.1:p.Ser1597=
NM_001374828.1:c.4909T= MANE Select	NP_001361757.1:p.Ser1637=
NM_017519.3:c.4750T=	NP_059989.3:p.Ser1584=