Canonical Allele Identifier: CA366241295

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4568A>C	ENSP00000055163.8:p.Gln1523Pro
ENST00000414678.8:c.4637A>C	ENSP00000412835.3:p.Gln1546Pro
ENST00000637015.2:c.4856A>C	ENSP00000489729.2:p.Gln1619Pro
ENST00000346085.10:c.4607A>C	ENSP00000344546.5:p.Gln1536Pro
ENST00000350026.10:c.4319A>C	ENSP00000055163.7:p.Gln1440Pro
ENST00000414678.7:c.2885A>C	ENSP00000412835.2:p.Gln962Pro
ENST00000635849.1:c.2048A>C	ENSP00000490948.1:p.Gln683Pro
ENST00000635957.1:c.1679A>C	ENSP00000490385.1:p.Gln560Pro
ENST00000636227.1:n.3190A>C
ENST00000636254.1:n.647A>C
ENST00000636930.2:c.4727A>C MANE Select	ENSP00000490491.2:p.Gln1576Pro
ENST00000636940.1:n.2724A>C
ENST00000637015.1:c.2095A>C
ENST00000637568.1:c.2009A>C
ENST00000637741.1:n.1393A>C
ENST00000637810.1:c.2069A>C	ENSP00000489636.1:p.Gln690Pro
ENST00000637904.1:c.2228A>C	ENSP00000490550.1:p.Gln743Pro
ENST00000647938.1:c.4358A>C	ENSP00000498155.1:p.Gln1453Pro
ENST00000346085.9:c.4358A>C	ENSP00000344546.4:p.Gln1453Pro
ENST00000350026.9:c.4319A>C	ENSP00000055163.7:p.Gln1440Pro
ENST00000414678.6:c.2885A>C	ENSP00000412835.2:p.Gln962Pro
NM_017519.2:c.4319A>C	NP_059989.2:p.Gln1440Pro
NM_020732.3:c.4358A>C	NP_065783.3:p.Gln1453Pro
XM_005267069.3:c.4478A>C	XP_005267126.2:p.Gln1493Pro
XM_011535984.1:c.3557A>C	XP_011534286.1:p.Gln1186Pro
XM_011535985.1:c.3377A>C	XP_011534287.1:p.Gln1126Pro
XM_011535986.1:c.3137A>C	XP_011534288.1:p.Gln1046Pro
XM_011535987.1:c.2756A>C	XP_011534289.1:p.Gln919Pro
XM_011535988.1:c.1619A>C	XP_011534290.1:p.Gln540Pro
NM_001346813.1:c.4478A>C	NP_001333742.1:p.Gln1493Pro
NM_001363725.1:c.2228A>C	NP_001350654.1:p.Gln743Pro
XM_011535984.2:c.4688A>C	XP_011534286.2:p.Gln1563Pro
XM_011535988.3:c.1619A>C	XP_011534290.1:p.Gln540Pro
XM_017011103.2:c.4589A>C	XP_016866592.1:p.Gln1530Pro
XM_017011104.1:c.4559A>C	XP_016866593.1:p.Gln1520Pro
XM_017011105.2:c.4529A>C	XP_016866594.1:p.Gln1510Pro
XM_017011106.2:c.4400A>C	XP_016866595.1:p.Gln1467Pro
XM_017011107.2:c.4379A>C	XP_016866596.1:p.Gln1460Pro
XR_002956289.1:n.4674A>C
NM_001363725.2:c.2228A>C	NP_001350654.1:p.Gln743Pro
NM_001371656.1:c.4607A>C	NP_001358585.1:p.Gln1536Pro
NM_001374820.1:c.4607A>C	NP_001361749.1:p.Gln1536Pro
NM_001374828.1:c.4727A>C MANE Select	NP_001361757.1:p.Gln1576Pro
NM_017519.3:c.4568A>C	NP_059989.3:p.Gln1523Pro