Canonical Allele Identifier: CA1675523085

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201164T= , CM000668.2:g.157201164T=	GRCh38
NC_000006.11:g.157522298T= , CM000668.1:g.157522298T=	GRCh37
NC_000006.10:g.157563990T=	NCBI36
NG_032093.1:g.428235T=
NG_032093.2:g.428235T=
NG_066624.1:g.430139T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4780T=	ENSP00000055163.8:p.Ser1594=
ENST00000414678.8:c.4849T=	ENSP00000412835.3:p.Ser1617=
ENST00000637015.2:c.5068T=	ENSP00000489729.2:p.Ser1690=
ENST00000346085.10:c.4819T=	ENSP00000344546.5:p.Ser1607=
ENST00000350026.10:c.4531T=	ENSP00000055163.7:p.Ser1511=
ENST00000414678.7:c.3097T=	ENSP00000412835.2:p.Ser1033=
ENST00000635849.1:c.2260T=	ENSP00000490948.1:p.Ser754=
ENST00000635957.1:c.1891T=	ENSP00000490385.1:p.Ser631=
ENST00000636227.1:n.3402T=
ENST00000636254.1:n.859T=
ENST00000636930.2:c.4939T= MANE Select	ENSP00000490491.2:p.Ser1647=
ENST00000636940.1:n.2936T=
ENST00000637015.1:c.2307T=
ENST00000637568.1:c.2221T=
ENST00000637741.1:n.1605T=
ENST00000637810.1:c.2281T=	ENSP00000489636.1:p.Ser761=
ENST00000637904.1:c.2440T=	ENSP00000490550.1:p.Ser814=
ENST00000647938.1:c.4570T=	ENSP00000498155.1:p.Ser1524=
ENST00000346085.9:c.4570T=	ENSP00000344546.4:p.Ser1524=
ENST00000350026.9:c.4531T=	ENSP00000055163.7:p.Ser1511=
ENST00000414678.6:c.3097T=	ENSP00000412835.2:p.Ser1033=
NM_017519.2:c.4531T=	NP_059989.2:p.Ser1511=
NM_020732.3:c.4570T=	NP_065783.3:p.Ser1524=
XM_005267069.3:c.4690T=	XP_005267126.2:p.Ser1564=
XM_011535984.1:c.3769T=	XP_011534286.1:p.Ser1257=
XM_011535985.1:c.3589T=	XP_011534287.1:p.Ser1197=
XM_011535986.1:c.3349T=	XP_011534288.1:p.Ser1117=
XM_011535987.1:c.2968T=	XP_011534289.1:p.Ser990=
XM_011535988.1:c.1831T=	XP_011534290.1:p.Ser611=
NM_001346813.1:c.4690T=	NP_001333742.1:p.Ser1564=
NM_001363725.1:c.2440T=	NP_001350654.1:p.Ser814=
XM_011535984.2:c.4900T=	XP_011534286.2:p.Ser1634=
XM_011535988.3:c.1831T=	XP_011534290.1:p.Ser611=
XM_017011103.2:c.4801T=	XP_016866592.1:p.Ser1601=
XM_017011104.1:c.4771T=	XP_016866593.1:p.Ser1591=
XM_017011105.2:c.4741T=	XP_016866594.1:p.Ser1581=
XM_017011106.2:c.4612T=	XP_016866595.1:p.Ser1538=
XM_017011107.2:c.4591T=	XP_016866596.1:p.Ser1531=
XR_002956289.1:n.4886T=
NM_001363725.2:c.2440T=	NP_001350654.1:p.Ser814=
NM_001371656.1:c.4819T=	NP_001358585.1:p.Ser1607=
NM_001374820.1:c.4819T=	NP_001361749.1:p.Ser1607=
NM_001374828.1:c.4939T= MANE Select	NP_001361757.1:p.Ser1647=
NM_017519.3:c.4780T=	NP_059989.3:p.Ser1594=