Canonical Allele Identifier: CA4067897

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206546G>A , CM000668.2:g.157206546G>A	GRCh38
NC_000006.11:g.157527680G>A , CM000668.1:g.157527680G>A	GRCh37
NC_000006.10:g.157569372G>A	NCBI36
NG_032093.1:g.433617G>A
NG_032093.2:g.433617G>A
NG_066624.1:g.435521G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.5774G>A MANE Select	NP_001361757.1:p.Arg1925Gln
ENST00000636930.2:c.5774G>A MANE Select	ENSP00000490491.2:p.Arg1925Gln
NM_001346813.1:c.5525G>A	NP_001333742.1:p.Arg1842Gln
NM_001363725.1:c.3275G>A	NP_001350654.1:p.Arg1092Gln
NM_001363725.2:c.3275G>A	NP_001350654.1:p.Arg1092Gln
NM_001371656.1:c.5654G>A	NP_001358585.1:p.Arg1885Gln
NM_001374820.1:c.5654G>A	NP_001361749.1:p.Arg1885Gln
NM_017519.2:c.5366G>A	NP_059989.2:p.Arg1789Gln
NM_017519.3:c.5615G>A	NP_059989.3:p.Arg1872Gln
NM_020732.3:c.5405G>A	NP_065783.3:p.Arg1802Gln
ENST00000346085.10:c.5654G>A	ENSP00000344546.5:p.Arg1885Gln
ENST00000346085.9:c.5405G>A	ENSP00000344546.4:p.Arg1802Gln
ENST00000350026.10:c.5366G>A	ENSP00000055163.7:p.Arg1789Gln
ENST00000350026.11:c.5615G>A	ENSP00000055163.8:p.Arg1872Gln
ENST00000350026.9:c.5366G>A	ENSP00000055163.7:p.Arg1789Gln
ENST00000414678.6:c.3932G>A	ENSP00000412835.2:p.Arg1311Gln
ENST00000414678.7:c.3932G>A	ENSP00000412835.2:p.Arg1311Gln
ENST00000414678.8:c.5684G>A	ENSP00000412835.3:p.Arg1895Gln
ENST00000635849.1:c.3095G>A	ENSP00000490948.1:p.Arg1032Gln
ENST00000635957.1:c.2726G>A	ENSP00000490385.1:p.Arg909Gln
ENST00000636227.1:n.4237G>A
ENST00000636254.1:n.1694G>A
ENST00000636940.1:n.3771G>A
ENST00000637015.1:c.3142G>A
ENST00000637015.2:c.5903G>A	ENSP00000489729.2:p.Arg1968Gln
ENST00000637568.1:c.3056G>A
ENST00000637741.1:n.2440G>A
ENST00000637810.1:c.3116G>A	ENSP00000489636.1:p.Arg1039Gln
ENST00000637904.1:c.3275G>A	ENSP00000490550.1:p.Arg1092Gln
ENST00000637933.1:n.2889G>A
ENST00000647938.1:c.5405G>A	ENSP00000498155.1:p.Arg1802Gln
XM_005267069.3:c.5525G>A	XP_005267126.2:p.Arg1842Gln
XM_011535984.1:c.4604G>A	XP_011534286.1:p.Arg1535Gln
XM_011535984.2:c.5735G>A	XP_011534286.2:p.Arg1912Gln
XM_011535985.1:c.4424G>A	XP_011534287.1:p.Arg1475Gln
XM_011535986.1:c.4184G>A	XP_011534288.1:p.Arg1395Gln
XM_011535987.1:c.3803G>A	XP_011534289.1:p.Arg1268Gln
XM_011535988.1:c.2666G>A	XP_011534290.1:p.Arg889Gln
XM_011535988.3:c.2666G>A	XP_011534290.1:p.Arg889Gln
XM_017011103.2:c.5636G>A	XP_016866592.1:p.Arg1879Gln
XM_017011104.1:c.5606G>A	XP_016866593.1:p.Arg1869Gln
XM_017011105.2:c.5576G>A	XP_016866594.1:p.Arg1859Gln
XM_017011106.2:c.5447G>A	XP_016866595.1:p.Arg1816Gln
XM_017011107.2:c.5426G>A	XP_016866596.1:p.Arg1809Gln
XR_002956289.1:n.5721G>A