Canonical Allele Identifier: CA366240795

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200747A>T , CM000668.2:g.157200747A>T	GRCh38
NC_000006.11:g.157521881A>T , CM000668.1:g.157521881A>T	GRCh37
NC_000006.10:g.157563573A>T	NCBI36
NG_032093.1:g.427818A>T
NG_032093.2:g.427818A>T
NG_066624.1:g.429722A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4363A>T	ENSP00000055163.8:p.Lys1455Ter
ENST00000414678.8:c.4432A>T	ENSP00000412835.3:p.Lys1478Ter
ENST00000637015.2:c.4651A>T	ENSP00000489729.2:p.Lys1551Ter
ENST00000346085.10:c.4402A>T	ENSP00000344546.5:p.Lys1468Ter
ENST00000350026.10:c.4114A>T	ENSP00000055163.7:p.Lys1372Ter
ENST00000414678.7:c.2680A>T	ENSP00000412835.2:p.Lys894Ter
ENST00000635849.1:c.1843A>T	ENSP00000490948.1:p.Lys615Ter
ENST00000635957.1:c.1474A>T	ENSP00000490385.1:p.Lys492Ter
ENST00000636227.1:n.2985A>T
ENST00000636254.1:n.442A>T
ENST00000636930.2:c.4522A>T MANE Select	ENSP00000490491.2:p.Lys1508Ter
ENST00000636940.1:n.2519A>T
ENST00000637015.1:c.1890A>T
ENST00000637568.1:c.1804A>T
ENST00000637741.1:n.1188A>T
ENST00000637810.1:c.1864A>T	ENSP00000489636.1:p.Lys622Ter
ENST00000637904.1:c.2023A>T	ENSP00000490550.1:p.Lys675Ter
ENST00000647938.1:c.4153A>T	ENSP00000498155.1:p.Lys1385Ter
ENST00000346085.9:c.4153A>T	ENSP00000344546.4:p.Lys1385Ter
ENST00000350026.9:c.4114A>T	ENSP00000055163.7:p.Lys1372Ter
ENST00000414678.6:c.2680A>T	ENSP00000412835.2:p.Lys894Ter
NM_017519.2:c.4114A>T	NP_059989.2:p.Lys1372Ter
NM_020732.3:c.4153A>T	NP_065783.3:p.Lys1385Ter
XM_005267069.3:c.4273A>T	XP_005267126.2:p.Lys1425Ter
XM_011535984.1:c.3352A>T	XP_011534286.1:p.Lys1118Ter
XM_011535985.1:c.3172A>T	XP_011534287.1:p.Lys1058Ter
XM_011535986.1:c.2932A>T	XP_011534288.1:p.Lys978Ter
XM_011535987.1:c.2551A>T	XP_011534289.1:p.Lys851Ter
XM_011535988.1:c.1414A>T	XP_011534290.1:p.Lys472Ter
NM_001346813.1:c.4273A>T	NP_001333742.1:p.Lys1425Ter
NM_001363725.1:c.2023A>T	NP_001350654.1:p.Lys675Ter
XM_011535984.2:c.4483A>T	XP_011534286.2:p.Lys1495Ter
XM_011535988.3:c.1414A>T	XP_011534290.1:p.Lys472Ter
XM_017011103.2:c.4384A>T	XP_016866592.1:p.Lys1462Ter
XM_017011104.1:c.4354A>T	XP_016866593.1:p.Lys1452Ter
XM_017011105.2:c.4324A>T	XP_016866594.1:p.Lys1442Ter
XM_017011106.2:c.4195A>T	XP_016866595.1:p.Lys1399Ter
XM_017011107.2:c.4174A>T	XP_016866596.1:p.Lys1392Ter
XR_002956289.1:n.4469A>T
NM_001363725.2:c.2023A>T	NP_001350654.1:p.Lys675Ter
NM_001371656.1:c.4402A>T	NP_001358585.1:p.Lys1468Ter
NM_001374820.1:c.4402A>T	NP_001361749.1:p.Lys1468Ter
NM_001374828.1:c.4522A>T MANE Select	NP_001361757.1:p.Lys1508Ter
NM_017519.3:c.4363A>T	NP_059989.3:p.Lys1455Ter