Canonical Allele Identifier: CA4067605

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196312G>A , CM000668.2:g.157196312G>A	GRCh38
NC_000006.11:g.157517446G>A , CM000668.1:g.157517446G>A	GRCh37
NC_000006.10:g.157559138G>A	NCBI36
NG_032093.1:g.423383G>A
NG_032093.2:g.423383G>A
NG_066624.1:g.425287G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4379G>A MANE Select	NP_001361757.1:p.Arg1460Gln
ENST00000636930.2:c.4379G>A MANE Select	ENSP00000490491.2:p.Arg1460Gln
NM_001346813.1:c.4130G>A	NP_001333742.1:p.Arg1377Gln
NM_001363725.1:c.1880G>A	NP_001350654.1:p.Arg627Gln
NM_001363725.2:c.1880G>A	NP_001350654.1:p.Arg627Gln
NM_001371656.1:c.4259G>A	NP_001358585.1:p.Arg1420Gln
NM_001374820.1:c.4259G>A	NP_001361749.1:p.Arg1420Gln
NM_017519.2:c.3971G>A	NP_059989.2:p.Arg1324Gln
NM_017519.3:c.4220G>A	NP_059989.3:p.Arg1407Gln
NM_020732.3:c.4010G>A	NP_065783.3:p.Arg1337Gln
ENST00000346085.10:c.4259G>A	ENSP00000344546.5:p.Arg1420Gln
ENST00000346085.9:c.4010G>A	ENSP00000344546.4:p.Arg1337Gln
ENST00000350026.10:c.3971G>A	ENSP00000055163.7:p.Arg1324Gln
ENST00000350026.11:c.4220G>A	ENSP00000055163.8:p.Arg1407Gln
ENST00000350026.9:c.3971G>A	ENSP00000055163.7:p.Arg1324Gln
ENST00000414678.6:c.2537G>A	ENSP00000412835.2:p.Arg846Gln
ENST00000414678.7:c.2537G>A	ENSP00000412835.2:p.Arg846Gln
ENST00000414678.8:c.4289G>A	ENSP00000412835.3:p.Arg1430Gln
ENST00000635849.1:c.1700G>A	ENSP00000490948.1:p.Arg567Gln
ENST00000635957.1:c.1331G>A	ENSP00000490385.1:p.Arg444Gln
ENST00000636227.1:n.2842G>A
ENST00000636940.1:n.2376G>A
ENST00000637015.1:c.1747G>A
ENST00000637015.2:c.4508G>A	ENSP00000489729.2:p.Arg1503Gln
ENST00000637568.1:c.1661G>A
ENST00000637741.1:n.1045G>A
ENST00000637810.1:c.1721G>A	ENSP00000489636.1:p.Arg574Gln
ENST00000637904.1:c.1880G>A	ENSP00000490550.1:p.Arg627Gln
ENST00000647938.1:c.4010G>A	ENSP00000498155.1:p.Arg1337Gln
XM_005267069.3:c.4130G>A	XP_005267126.2:p.Arg1377Gln
XM_011535984.1:c.3209G>A	XP_011534286.1:p.Arg1070Gln
XM_011535984.2:c.4340G>A	XP_011534286.2:p.Arg1447Gln
XM_011535985.1:c.3029G>A	XP_011534287.1:p.Arg1010Gln
XM_011535986.1:c.2789G>A	XP_011534288.1:p.Arg930Gln
XM_011535987.1:c.2408G>A	XP_011534289.1:p.Arg803Gln
XM_011535988.1:c.1271G>A	XP_011534290.1:p.Arg424Gln
XM_011535988.3:c.1271G>A	XP_011534290.1:p.Arg424Gln
XM_017011103.2:c.4241G>A	XP_016866592.1:p.Arg1414Gln
XM_017011104.1:c.4211G>A	XP_016866593.1:p.Arg1404Gln
XM_017011105.2:c.4181G>A	XP_016866594.1:p.Arg1394Gln
XM_017011106.2:c.4052G>A	XP_016866595.1:p.Arg1351Gln
XM_017011107.2:c.4031G>A	XP_016866596.1:p.Arg1344Gln
XR_002956289.1:n.4423G>A