Canonical Allele Identifier: CA366240741

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200735G>A , CM000668.2:g.157200735G>A	GRCh38
NC_000006.11:g.157521869G>A , CM000668.1:g.157521869G>A	GRCh37
NC_000006.10:g.157563561G>A	NCBI36
NG_032093.1:g.427806G>A
NG_032093.2:g.427806G>A
NG_066624.1:g.429710G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4351G>A	ENSP00000055163.8:p.Gly1451Arg
ENST00000414678.8:c.4420G>A	ENSP00000412835.3:p.Gly1474Arg
ENST00000637015.2:c.4639G>A	ENSP00000489729.2:p.Gly1547Arg
ENST00000346085.10:c.4390G>A	ENSP00000344546.5:p.Gly1464Arg
ENST00000350026.10:c.4102G>A	ENSP00000055163.7:p.Gly1368Arg
ENST00000414678.7:c.2668G>A	ENSP00000412835.2:p.Gly890Arg
ENST00000635849.1:c.1831G>A	ENSP00000490948.1:p.Gly611Arg
ENST00000635957.1:c.1462G>A	ENSP00000490385.1:p.Gly488Arg
ENST00000636227.1:n.2973G>A
ENST00000636254.1:n.430G>A
ENST00000636930.2:c.4510G>A MANE Select	ENSP00000490491.2:p.Gly1504Arg
ENST00000636940.1:n.2507G>A
ENST00000637015.1:c.1878G>A
ENST00000637568.1:c.1792G>A
ENST00000637741.1:n.1176G>A
ENST00000637810.1:c.1852G>A	ENSP00000489636.1:p.Gly618Arg
ENST00000637904.1:c.2011G>A	ENSP00000490550.1:p.Gly671Arg
ENST00000647938.1:c.4141G>A	ENSP00000498155.1:p.Gly1381Arg
ENST00000346085.9:c.4141G>A	ENSP00000344546.4:p.Gly1381Arg
ENST00000350026.9:c.4102G>A	ENSP00000055163.7:p.Gly1368Arg
ENST00000414678.6:c.2668G>A	ENSP00000412835.2:p.Gly890Arg
NM_017519.2:c.4102G>A	NP_059989.2:p.Gly1368Arg
NM_020732.3:c.4141G>A	NP_065783.3:p.Gly1381Arg
XM_005267069.3:c.4261G>A	XP_005267126.2:p.Gly1421Arg
XM_011535984.1:c.3340G>A	XP_011534286.1:p.Gly1114Arg
XM_011535985.1:c.3160G>A	XP_011534287.1:p.Gly1054Arg
XM_011535986.1:c.2920G>A	XP_011534288.1:p.Gly974Arg
XM_011535987.1:c.2539G>A	XP_011534289.1:p.Gly847Arg
XM_011535988.1:c.1402G>A	XP_011534290.1:p.Gly468Arg
NM_001346813.1:c.4261G>A	NP_001333742.1:p.Gly1421Arg
NM_001363725.1:c.2011G>A	NP_001350654.1:p.Gly671Arg
XM_011535984.2:c.4471G>A	XP_011534286.2:p.Gly1491Arg
XM_011535988.3:c.1402G>A	XP_011534290.1:p.Gly468Arg
XM_017011103.2:c.4372G>A	XP_016866592.1:p.Gly1458Arg
XM_017011104.1:c.4342G>A	XP_016866593.1:p.Gly1448Arg
XM_017011105.2:c.4312G>A	XP_016866594.1:p.Gly1438Arg
XM_017011106.2:c.4183G>A	XP_016866595.1:p.Gly1395Arg
XM_017011107.2:c.4162G>A	XP_016866596.1:p.Gly1388Arg
XR_002956289.1:n.4457G>A
NM_001363725.2:c.2011G>A	NP_001350654.1:p.Gly671Arg
NM_001371656.1:c.4390G>A	NP_001358585.1:p.Gly1464Arg
NM_001374820.1:c.4390G>A	NP_001361749.1:p.Gly1464Arg
NM_001374828.1:c.4510G>A MANE Select	NP_001361757.1:p.Gly1504Arg
NM_017519.3:c.4351G>A	NP_059989.3:p.Gly1451Arg