Canonical Allele Identifier: CA366235333

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190129C>T , CM000668.2:g.157190129C>T	GRCh38
NC_000006.11:g.157511263C>T , CM000668.1:g.157511263C>T	GRCh37
NC_000006.10:g.157552955C>T	NCBI36
NG_032093.1:g.417200C>T
NG_032093.2:g.417200C>T
NG_066624.1:g.419104C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4150C>T MANE Select	NP_001361757.1:p.Gln1384Ter
ENST00000636930.2:c.4150C>T MANE Select	ENSP00000490491.2:p.Gln1384Ter
NM_001346813.1:c.3901C>T	NP_001333742.1:p.Gln1301Ter
NM_001363725.1:c.1651C>T	NP_001350654.1:p.Gln551Ter
NM_001363725.2:c.1651C>T	NP_001350654.1:p.Gln551Ter
NM_001371656.1:c.4030C>T	NP_001358585.1:p.Gln1344Ter
NM_001374820.1:c.4030C>T	NP_001361749.1:p.Gln1344Ter
NM_017519.2:c.3742C>T	NP_059989.2:p.Gln1248Ter
NM_017519.3:c.3991C>T	NP_059989.3:p.Gln1331Ter
NM_020732.3:c.3781C>T	NP_065783.3:p.Gln1261Ter
ENST00000346085.10:c.4030C>T	ENSP00000344546.5:p.Gln1344Ter
ENST00000346085.9:c.3781C>T	ENSP00000344546.4:p.Gln1261Ter
ENST00000350026.10:c.3742C>T	ENSP00000055163.7:p.Gln1248Ter
ENST00000350026.11:c.3991C>T	ENSP00000055163.8:p.Gln1331Ter
ENST00000350026.9:c.3742C>T	ENSP00000055163.7:p.Gln1248Ter
ENST00000414678.6:c.2308C>T	ENSP00000412835.2:p.Gln770Ter
ENST00000414678.7:c.2308C>T	ENSP00000412835.2:p.Gln770Ter
ENST00000414678.8:c.4060C>T	ENSP00000412835.3:p.Gln1354Ter
ENST00000635849.1:c.1471C>T	ENSP00000490948.1:p.Gln491Ter
ENST00000635957.1:c.1102C>T	ENSP00000490385.1:p.Gln368Ter
ENST00000636940.1:n.2147C>T
ENST00000637015.1:c.1518C>T
ENST00000637015.2:c.4279C>T	ENSP00000489729.2:p.Gln1427Ter
ENST00000637568.1:c.1432C>T
ENST00000637741.1:n.816C>T
ENST00000637810.1:c.1492C>T	ENSP00000489636.1:p.Gln498Ter
ENST00000637904.1:c.1651C>T	ENSP00000490550.1:p.Gln551Ter
ENST00000647938.1:c.3781C>T	ENSP00000498155.1:p.Gln1261Ter
XM_005267069.3:c.3901C>T	XP_005267126.2:p.Gln1301Ter
XM_011535984.1:c.2980C>T	XP_011534286.1:p.Gln994Ter
XM_011535984.2:c.4111C>T	XP_011534286.2:p.Gln1371Ter
XM_011535985.1:c.2800C>T	XP_011534287.1:p.Gln934Ter
XM_011535986.1:c.2560C>T	XP_011534288.1:p.Gln854Ter
XM_011535987.1:c.2179C>T	XP_011534289.1:p.Gln727Ter
XM_011535988.1:c.1042C>T	XP_011534290.1:p.Gln348Ter
XM_011535988.3:c.1042C>T	XP_011534290.1:p.Gln348Ter
XM_017011103.2:c.4012C>T	XP_016866592.1:p.Gln1338Ter
XM_017011104.1:c.3982C>T	XP_016866593.1:p.Gln1328Ter
XM_017011105.2:c.3952C>T	XP_016866594.1:p.Gln1318Ter
XM_017011106.2:c.3823C>T	XP_016866595.1:p.Gln1275Ter
XM_017011107.2:c.3802C>T	XP_016866596.1:p.Gln1268Ter
XR_002956289.1:n.4194C>T