Canonical Allele Identifier: CA366241296

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522086A>T (hg19) ; chr6:g.157200952A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200952A>T , CM000668.2:g.157200952A>T	GRCh38
NC_000006.11:g.157522086A>T , CM000668.1:g.157522086A>T	GRCh37
NC_000006.10:g.157563778A>T	NCBI36
NG_032093.1:g.428023A>T
NG_032093.2:g.428023A>T
NG_066624.1:g.429927A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4568A>T	ENSP00000055163.8:p.Gln1523Leu
ENST00000414678.8:c.4637A>T	ENSP00000412835.3:p.Gln1546Leu
ENST00000637015.2:c.4856A>T	ENSP00000489729.2:p.Gln1619Leu
ENST00000346085.10:c.4607A>T	ENSP00000344546.5:p.Gln1536Leu
ENST00000350026.10:c.4319A>T	ENSP00000055163.7:p.Gln1440Leu
ENST00000414678.7:c.2885A>T	ENSP00000412835.2:p.Gln962Leu
ENST00000635849.1:c.2048A>T	ENSP00000490948.1:p.Gln683Leu
ENST00000635957.1:c.1679A>T	ENSP00000490385.1:p.Gln560Leu
ENST00000636227.1:n.3190A>T
ENST00000636254.1:n.647A>T
ENST00000636930.2:c.4727A>T MANE Select	ENSP00000490491.2:p.Gln1576Leu
ENST00000636940.1:n.2724A>T
ENST00000637015.1:c.2095A>T
ENST00000637568.1:c.2009A>T
ENST00000637741.1:n.1393A>T
ENST00000637810.1:c.2069A>T	ENSP00000489636.1:p.Gln690Leu
ENST00000637904.1:c.2228A>T	ENSP00000490550.1:p.Gln743Leu
ENST00000647938.1:c.4358A>T	ENSP00000498155.1:p.Gln1453Leu
ENST00000346085.9:c.4358A>T	ENSP00000344546.4:p.Gln1453Leu
ENST00000350026.9:c.4319A>T	ENSP00000055163.7:p.Gln1440Leu
ENST00000414678.6:c.2885A>T	ENSP00000412835.2:p.Gln962Leu
NM_017519.2:c.4319A>T	NP_059989.2:p.Gln1440Leu
NM_020732.3:c.4358A>T	NP_065783.3:p.Gln1453Leu
XM_005267069.3:c.4478A>T	XP_005267126.2:p.Gln1493Leu
XM_011535984.1:c.3557A>T	XP_011534286.1:p.Gln1186Leu
XM_011535985.1:c.3377A>T	XP_011534287.1:p.Gln1126Leu
XM_011535986.1:c.3137A>T	XP_011534288.1:p.Gln1046Leu
XM_011535987.1:c.2756A>T	XP_011534289.1:p.Gln919Leu
XM_011535988.1:c.1619A>T	XP_011534290.1:p.Gln540Leu
NM_001346813.1:c.4478A>T	NP_001333742.1:p.Gln1493Leu
NM_001363725.1:c.2228A>T	NP_001350654.1:p.Gln743Leu
XM_011535984.2:c.4688A>T	XP_011534286.2:p.Gln1563Leu
XM_011535988.3:c.1619A>T	XP_011534290.1:p.Gln540Leu
XM_017011103.2:c.4589A>T	XP_016866592.1:p.Gln1530Leu
XM_017011104.1:c.4559A>T	XP_016866593.1:p.Gln1520Leu
XM_017011105.2:c.4529A>T	XP_016866594.1:p.Gln1510Leu
XM_017011106.2:c.4400A>T	XP_016866595.1:p.Gln1467Leu
XM_017011107.2:c.4379A>T	XP_016866596.1:p.Gln1460Leu
XR_002956289.1:n.4674A>T
NM_001363725.2:c.2228A>T	NP_001350654.1:p.Gln743Leu
NM_001371656.1:c.4607A>T	NP_001358585.1:p.Gln1536Leu
NM_001374820.1:c.4607A>T	NP_001361749.1:p.Gln1536Leu
NM_001374828.1:c.4727A>T MANE Select	NP_001361757.1:p.Gln1576Leu
NM_017519.3:c.4568A>T	NP_059989.3:p.Gln1523Leu