Canonical Allele Identifier: CA366238872

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196311C>T , CM000668.2:g.157196311C>T	GRCh38
NC_000006.11:g.157517445C>T , CM000668.1:g.157517445C>T	GRCh37
NC_000006.10:g.157559137C>T	NCBI36
NG_032093.1:g.423382C>T
NG_032093.2:g.423382C>T
NG_066624.1:g.425286C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4378C>T MANE Select	NP_001361757.1:p.Arg1460Ter
ENST00000636930.2:c.4378C>T MANE Select	ENSP00000490491.2:p.Arg1460Ter
NM_001346813.1:c.4129C>T	NP_001333742.1:p.Arg1377Ter
NM_001363725.1:c.1879C>T	NP_001350654.1:p.Arg627Ter
NM_001363725.2:c.1879C>T	NP_001350654.1:p.Arg627Ter
NM_001371656.1:c.4258C>T	NP_001358585.1:p.Arg1420Ter
NM_001374820.1:c.4258C>T	NP_001361749.1:p.Arg1420Ter
NM_017519.2:c.3970C>T	NP_059989.2:p.Arg1324Ter
NM_017519.3:c.4219C>T	NP_059989.3:p.Arg1407Ter
NM_020732.3:c.4009C>T	NP_065783.3:p.Arg1337Ter
ENST00000346085.10:c.4258C>T	ENSP00000344546.5:p.Arg1420Ter
ENST00000346085.9:c.4009C>T	ENSP00000344546.4:p.Arg1337Ter
ENST00000350026.10:c.3970C>T	ENSP00000055163.7:p.Arg1324Ter
ENST00000350026.11:c.4219C>T	ENSP00000055163.8:p.Arg1407Ter
ENST00000350026.9:c.3970C>T	ENSP00000055163.7:p.Arg1324Ter
ENST00000414678.6:c.2536C>T	ENSP00000412835.2:p.Arg846Ter
ENST00000414678.7:c.2536C>T	ENSP00000412835.2:p.Arg846Ter
ENST00000414678.8:c.4288C>T	ENSP00000412835.3:p.Arg1430Ter
ENST00000635849.1:c.1699C>T	ENSP00000490948.1:p.Arg567Ter
ENST00000635957.1:c.1330C>T	ENSP00000490385.1:p.Arg444Ter
ENST00000636227.1:n.2841C>T
ENST00000636940.1:n.2375C>T
ENST00000637015.1:c.1746C>T
ENST00000637015.2:c.4507C>T	ENSP00000489729.2:p.Arg1503Ter
ENST00000637568.1:c.1660C>T
ENST00000637741.1:n.1044C>T
ENST00000637810.1:c.1720C>T	ENSP00000489636.1:p.Arg574Ter
ENST00000637904.1:c.1879C>T	ENSP00000490550.1:p.Arg627Ter
ENST00000647938.1:c.4009C>T	ENSP00000498155.1:p.Arg1337Ter
XM_005267069.3:c.4129C>T	XP_005267126.2:p.Arg1377Ter
XM_011535984.1:c.3208C>T	XP_011534286.1:p.Arg1070Ter
XM_011535984.2:c.4339C>T	XP_011534286.2:p.Arg1447Ter
XM_011535985.1:c.3028C>T	XP_011534287.1:p.Arg1010Ter
XM_011535986.1:c.2788C>T	XP_011534288.1:p.Arg930Ter
XM_011535987.1:c.2407C>T	XP_011534289.1:p.Arg803Ter
XM_011535988.1:c.1270C>T	XP_011534290.1:p.Arg424Ter
XM_011535988.3:c.1270C>T	XP_011534290.1:p.Arg424Ter
XM_017011103.2:c.4240C>T	XP_016866592.1:p.Arg1414Ter
XM_017011104.1:c.4210C>T	XP_016866593.1:p.Arg1404Ter
XM_017011105.2:c.4180C>T	XP_016866594.1:p.Arg1394Ter
XM_017011106.2:c.4051C>T	XP_016866595.1:p.Arg1351Ter
XM_017011107.2:c.4030C>T	XP_016866596.1:p.Arg1344Ter
XR_002956289.1:n.4422C>T