Canonical Allele Identifier: CA366242563

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235948
• MyVariant Identifiers: chr6:g.157522463A>T (hg19) ; chr6:g.157201329A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201329A>T , CM000668.2:g.157201329A>T	GRCh38
NC_000006.11:g.157522463A>T , CM000668.1:g.157522463A>T	GRCh37
NC_000006.10:g.157564155A>T	NCBI36
NG_032093.1:g.428400A>T
NG_032093.2:g.428400A>T
NG_066624.1:g.430304A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4945A>T	ENSP00000055163.8:p.Lys1649Ter
ENST00000414678.8:c.5014A>T	ENSP00000412835.3:p.Lys1672Ter
ENST00000637015.2:c.5233A>T	ENSP00000489729.2:p.Lys1745Ter
ENST00000346085.10:c.4984A>T	ENSP00000344546.5:p.Lys1662Ter
ENST00000350026.10:c.4696A>T	ENSP00000055163.7:p.Lys1566Ter
ENST00000414678.7:c.3262A>T	ENSP00000412835.2:p.Lys1088Ter
ENST00000635849.1:c.2425A>T	ENSP00000490948.1:p.Lys809Ter
ENST00000635957.1:c.2056A>T	ENSP00000490385.1:p.Lys686Ter
ENST00000636227.1:n.3567A>T
ENST00000636254.1:n.1024A>T
ENST00000636930.2:c.5104A>T MANE Select	ENSP00000490491.2:p.Lys1702Ter
ENST00000636940.1:n.3101A>T
ENST00000637015.1:c.2472A>T
ENST00000637568.1:c.2386A>T
ENST00000637741.1:n.1770A>T
ENST00000637810.1:c.2446A>T	ENSP00000489636.1:p.Lys816Ter
ENST00000637904.1:c.2605A>T	ENSP00000490550.1:p.Lys869Ter
ENST00000647938.1:c.4735A>T	ENSP00000498155.1:p.Lys1579Ter
ENST00000346085.9:c.4735A>T	ENSP00000344546.4:p.Lys1579Ter
ENST00000350026.9:c.4696A>T	ENSP00000055163.7:p.Lys1566Ter
ENST00000414678.6:c.3262A>T	ENSP00000412835.2:p.Lys1088Ter
NM_017519.2:c.4696A>T	NP_059989.2:p.Lys1566Ter
NM_020732.3:c.4735A>T	NP_065783.3:p.Lys1579Ter
XM_005267069.3:c.4855A>T	XP_005267126.2:p.Lys1619Ter
XM_011535984.1:c.3934A>T	XP_011534286.1:p.Lys1312Ter
XM_011535985.1:c.3754A>T	XP_011534287.1:p.Lys1252Ter
XM_011535986.1:c.3514A>T	XP_011534288.1:p.Lys1172Ter
XM_011535987.1:c.3133A>T	XP_011534289.1:p.Lys1045Ter
XM_011535988.1:c.1996A>T	XP_011534290.1:p.Lys666Ter
NM_001346813.1:c.4855A>T	NP_001333742.1:p.Lys1619Ter
NM_001363725.1:c.2605A>T	NP_001350654.1:p.Lys869Ter
XM_011535984.2:c.5065A>T	XP_011534286.2:p.Lys1689Ter
XM_011535988.3:c.1996A>T	XP_011534290.1:p.Lys666Ter
XM_017011103.2:c.4966A>T	XP_016866592.1:p.Lys1656Ter
XM_017011104.1:c.4936A>T	XP_016866593.1:p.Lys1646Ter
XM_017011105.2:c.4906A>T	XP_016866594.1:p.Lys1636Ter
XM_017011106.2:c.4777A>T	XP_016866595.1:p.Lys1593Ter
XM_017011107.2:c.4756A>T	XP_016866596.1:p.Lys1586Ter
XR_002956289.1:n.5051A>T
NM_001363725.2:c.2605A>T	NP_001350654.1:p.Lys869Ter
NM_001371656.1:c.4984A>T	NP_001358585.1:p.Lys1662Ter
NM_001374820.1:c.4984A>T	NP_001361749.1:p.Lys1662Ter
NM_001374828.1:c.5104A>T MANE Select	NP_001361757.1:p.Lys1702Ter
NM_017519.3:c.4945A>T	NP_059989.3:p.Lys1649Ter