Canonical Allele Identifier: CA4067773

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201465G>A , CM000668.2:g.157201465G>A	GRCh38
NC_000006.11:g.157522599G>A , CM000668.1:g.157522599G>A	GRCh37
NC_000006.10:g.157564291G>A	NCBI36
NG_032093.1:g.428536G>A
NG_032093.2:g.428536G>A
NG_066624.1:g.430440G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.5240G>A MANE Select	NP_001361757.1:p.Arg1747Gln
ENST00000636930.2:c.5240G>A MANE Select	ENSP00000490491.2:p.Arg1747Gln
NM_001346813.1:c.4991G>A	NP_001333742.1:p.Arg1664Gln
NM_001363725.1:c.2741G>A	NP_001350654.1:p.Arg914Gln
NM_001363725.2:c.2741G>A	NP_001350654.1:p.Arg914Gln
NM_001371656.1:c.5120G>A	NP_001358585.1:p.Arg1707Gln
NM_001374820.1:c.5120G>A	NP_001361749.1:p.Arg1707Gln
NM_017519.2:c.4832G>A	NP_059989.2:p.Arg1611Gln
NM_017519.3:c.5081G>A	NP_059989.3:p.Arg1694Gln
NM_020732.3:c.4871G>A	NP_065783.3:p.Arg1624Gln
ENST00000346085.10:c.5120G>A	ENSP00000344546.5:p.Arg1707Gln
ENST00000346085.9:c.4871G>A	ENSP00000344546.4:p.Arg1624Gln
ENST00000350026.10:c.4832G>A	ENSP00000055163.7:p.Arg1611Gln
ENST00000350026.11:c.5081G>A	ENSP00000055163.8:p.Arg1694Gln
ENST00000350026.9:c.4832G>A	ENSP00000055163.7:p.Arg1611Gln
ENST00000414678.6:c.3398G>A	ENSP00000412835.2:p.Arg1133Gln
ENST00000414678.7:c.3398G>A	ENSP00000412835.2:p.Arg1133Gln
ENST00000414678.8:c.5150G>A	ENSP00000412835.3:p.Arg1717Gln
ENST00000635849.1:c.2561G>A	ENSP00000490948.1:p.Arg854Gln
ENST00000635957.1:c.2192G>A	ENSP00000490385.1:p.Arg731Gln
ENST00000636227.1:n.3703G>A
ENST00000636254.1:n.1160G>A
ENST00000636940.1:n.3237G>A
ENST00000637015.1:c.2608G>A
ENST00000637015.2:c.5369G>A	ENSP00000489729.2:p.Arg1790Gln
ENST00000637568.1:c.2522G>A
ENST00000637741.1:n.1906G>A
ENST00000637810.1:c.2582G>A	ENSP00000489636.1:p.Arg861Gln
ENST00000637904.1:c.2741G>A	ENSP00000490550.1:p.Arg914Gln
ENST00000647938.1:c.4871G>A	ENSP00000498155.1:p.Arg1624Gln
XM_005267069.3:c.4991G>A	XP_005267126.2:p.Arg1664Gln
XM_011535984.1:c.4070G>A	XP_011534286.1:p.Arg1357Gln
XM_011535984.2:c.5201G>A	XP_011534286.2:p.Arg1734Gln
XM_011535985.1:c.3890G>A	XP_011534287.1:p.Arg1297Gln
XM_011535986.1:c.3650G>A	XP_011534288.1:p.Arg1217Gln
XM_011535987.1:c.3269G>A	XP_011534289.1:p.Arg1090Gln
XM_011535988.1:c.2132G>A	XP_011534290.1:p.Arg711Gln
XM_011535988.3:c.2132G>A	XP_011534290.1:p.Arg711Gln
XM_017011103.2:c.5102G>A	XP_016866592.1:p.Arg1701Gln
XM_017011104.1:c.5072G>A	XP_016866593.1:p.Arg1691Gln
XM_017011105.2:c.5042G>A	XP_016866594.1:p.Arg1681Gln
XM_017011106.2:c.4913G>A	XP_016866595.1:p.Arg1638Gln
XM_017011107.2:c.4892G>A	XP_016866596.1:p.Arg1631Gln
XR_002956289.1:n.5187G>A