Canonical Allele Identifier: CA366248678

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207391G>T , CM000668.2:g.157207391G>T	GRCh38
NC_000006.11:g.157528525G>T , CM000668.1:g.157528525G>T	GRCh37
NC_000006.10:g.157570217G>T	NCBI36
NG_032093.1:g.434462G>T
NG_032093.2:g.434462G>T
NG_066624.1:g.436366G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6460G>T	ENSP00000055163.8:p.Glu2154Ter
ENST00000414678.8:c.6529G>T	ENSP00000412835.3:p.Glu2177Ter
ENST00000637015.2:c.6748G>T	ENSP00000489729.2:p.Glu2250Ter
ENST00000346085.10:c.6499G>T	ENSP00000344546.5:p.Glu2167Ter
ENST00000350026.10:c.6211G>T	ENSP00000055163.7:p.Glu2071Ter
ENST00000414678.7:c.4777G>T	ENSP00000412835.2:p.Glu1593Ter
ENST00000635849.1:c.3940G>T	ENSP00000490948.1:p.Glu1314Ter
ENST00000635928.1:c.775G>T	ENSP00000489717.1:p.Glu259Ter
ENST00000635957.1:c.3571G>T	ENSP00000490385.1:p.Glu1191Ter
ENST00000636227.1:n.5082G>T
ENST00000636254.1:n.2539G>T
ENST00000636930.2:c.6619G>T MANE Select	ENSP00000490491.2:p.Glu2207Ter
ENST00000636940.1:n.4616G>T
ENST00000637015.1:c.3987G>T
ENST00000637568.1:c.3901G>T
ENST00000637741.1:n.3285G>T
ENST00000637810.1:c.3961G>T	ENSP00000489636.1:p.Glu1321Ter
ENST00000637904.1:c.4120G>T	ENSP00000490550.1:p.Glu1374Ter
ENST00000637933.1:n.3734G>T
ENST00000647938.1:c.6250G>T	ENSP00000498155.1:p.Glu2084Ter
ENST00000346085.9:c.6250G>T	ENSP00000344546.4:p.Glu2084Ter
ENST00000350026.9:c.6211G>T	ENSP00000055163.7:p.Glu2071Ter
ENST00000414678.6:c.4777G>T	ENSP00000412835.2:p.Glu1593Ter
NM_017519.2:c.6211G>T	NP_059989.2:p.Glu2071Ter
NM_020732.3:c.6250G>T	NP_065783.3:p.Glu2084Ter
XM_005267069.3:c.6370G>T	XP_005267126.2:p.Glu2124Ter
XM_011535984.1:c.5449G>T	XP_011534286.1:p.Glu1817Ter
XM_011535985.1:c.5269G>T	XP_011534287.1:p.Glu1757Ter
XM_011535986.1:c.5029G>T	XP_011534288.1:p.Glu1677Ter
XM_011535987.1:c.4648G>T	XP_011534289.1:p.Glu1550Ter
XM_011535988.1:c.3511G>T	XP_011534290.1:p.Glu1171Ter
NM_001346813.1:c.6370G>T	NP_001333742.1:p.Glu2124Ter
NM_001363725.1:c.4120G>T	NP_001350654.1:p.Glu1374Ter
XM_011535984.2:c.6580G>T	XP_011534286.2:p.Glu2194Ter
XM_011535988.3:c.3511G>T	XP_011534290.1:p.Glu1171Ter
XM_017011103.2:c.6481G>T	XP_016866592.1:p.Glu2161Ter
XM_017011104.1:c.6451G>T	XP_016866593.1:p.Glu2151Ter
XM_017011105.2:c.6421G>T	XP_016866594.1:p.Glu2141Ter
XM_017011106.2:c.6292G>T	XP_016866595.1:p.Glu2098Ter
XM_017011107.2:c.6271G>T	XP_016866596.1:p.Glu2091Ter
XR_002956289.1:n.6566G>T
NM_001363725.2:c.4120G>T	NP_001350654.1:p.Glu1374Ter
NM_001371656.1:c.6499G>T	NP_001358585.1:p.Glu2167Ter
NM_001374820.1:c.6499G>T	NP_001361749.1:p.Glu2167Ter
NM_001374828.1:c.6619G>T MANE Select	NP_001361757.1:p.Glu2207Ter
NM_017519.3:c.6460G>T	NP_059989.3:p.Glu2154Ter