Canonical Allele Identifier: CA366241714

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374185
• MyVariant Identifiers: chr6:g.157522185A>T (hg19) ; chr6:g.157201051A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201051A>T , CM000668.2:g.157201051A>T	GRCh38
NC_000006.11:g.157522185A>T , CM000668.1:g.157522185A>T	GRCh37
NC_000006.10:g.157563877A>T	NCBI36
NG_032093.1:g.428122A>T
NG_032093.2:g.428122A>T
NG_066624.1:g.430026A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4667A>T	ENSP00000055163.8:p.Gln1556Leu
ENST00000414678.8:c.4736A>T	ENSP00000412835.3:p.Gln1579Leu
ENST00000637015.2:c.4955A>T	ENSP00000489729.2:p.Gln1652Leu
ENST00000346085.10:c.4706A>T	ENSP00000344546.5:p.Gln1569Leu
ENST00000350026.10:c.4418A>T	ENSP00000055163.7:p.Gln1473Leu
ENST00000414678.7:c.2984A>T	ENSP00000412835.2:p.Gln995Leu
ENST00000635849.1:c.2147A>T	ENSP00000490948.1:p.Gln716Leu
ENST00000635957.1:c.1778A>T	ENSP00000490385.1:p.Gln593Leu
ENST00000636227.1:n.3289A>T
ENST00000636254.1:n.746A>T
ENST00000636930.2:c.4826A>T MANE Select	ENSP00000490491.2:p.Gln1609Leu
ENST00000636940.1:n.2823A>T
ENST00000637015.1:c.2194A>T
ENST00000637568.1:c.2108A>T
ENST00000637741.1:n.1492A>T
ENST00000637810.1:c.2168A>T	ENSP00000489636.1:p.Gln723Leu
ENST00000637904.1:c.2327A>T	ENSP00000490550.1:p.Gln776Leu
ENST00000647938.1:c.4457A>T	ENSP00000498155.1:p.Gln1486Leu
ENST00000346085.9:c.4457A>T	ENSP00000344546.4:p.Gln1486Leu
ENST00000350026.9:c.4418A>T	ENSP00000055163.7:p.Gln1473Leu
ENST00000414678.6:c.2984A>T	ENSP00000412835.2:p.Gln995Leu
NM_017519.2:c.4418A>T	NP_059989.2:p.Gln1473Leu
NM_020732.3:c.4457A>T	NP_065783.3:p.Gln1486Leu
XM_005267069.3:c.4577A>T	XP_005267126.2:p.Gln1526Leu
XM_011535984.1:c.3656A>T	XP_011534286.1:p.Gln1219Leu
XM_011535985.1:c.3476A>T	XP_011534287.1:p.Gln1159Leu
XM_011535986.1:c.3236A>T	XP_011534288.1:p.Gln1079Leu
XM_011535987.1:c.2855A>T	XP_011534289.1:p.Gln952Leu
XM_011535988.1:c.1718A>T	XP_011534290.1:p.Gln573Leu
NM_001346813.1:c.4577A>T	NP_001333742.1:p.Gln1526Leu
NM_001363725.1:c.2327A>T	NP_001350654.1:p.Gln776Leu
XM_011535984.2:c.4787A>T	XP_011534286.2:p.Gln1596Leu
XM_011535988.3:c.1718A>T	XP_011534290.1:p.Gln573Leu
XM_017011103.2:c.4688A>T	XP_016866592.1:p.Gln1563Leu
XM_017011104.1:c.4658A>T	XP_016866593.1:p.Gln1553Leu
XM_017011105.2:c.4628A>T	XP_016866594.1:p.Gln1543Leu
XM_017011106.2:c.4499A>T	XP_016866595.1:p.Gln1500Leu
XM_017011107.2:c.4478A>T	XP_016866596.1:p.Gln1493Leu
XR_002956289.1:n.4773A>T
NM_001363725.2:c.2327A>T	NP_001350654.1:p.Gln776Leu
NM_001371656.1:c.4706A>T	NP_001358585.1:p.Gln1569Leu
NM_001374820.1:c.4706A>T	NP_001361749.1:p.Gln1569Leu
NM_001374828.1:c.4826A>T MANE Select	NP_001361757.1:p.Gln1609Leu
NM_017519.3:c.4667A>T	NP_059989.3:p.Gln1556Leu