Canonical Allele Identifier: CA1675542228

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198846G= , CM000668.2:g.157198846G=	GRCh38
NC_000006.11:g.157519980G= , CM000668.1:g.157519980G=	GRCh37
NC_000006.10:g.157561672G=	NCBI36
NG_032093.1:g.425917G=
NG_032093.2:g.425917G=
NG_066624.1:g.427821G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4259G=	ENSP00000055163.8:p.Gly1420=
ENST00000414678.8:c.4328G=	ENSP00000412835.3:p.Gly1443=
ENST00000637015.2:c.4547G=	ENSP00000489729.2:p.Gly1516=
ENST00000346085.10:c.4298G=	ENSP00000344546.5:p.Gly1433=
ENST00000350026.10:c.4010G=	ENSP00000055163.7:p.Gly1337=
ENST00000414678.7:c.2576G=	ENSP00000412835.2:p.Gly859=
ENST00000635849.1:c.1739G=	ENSP00000490948.1:p.Gly580=
ENST00000635957.1:c.1370G=	ENSP00000490385.1:p.Gly457=
ENST00000636227.1:n.2881G=
ENST00000636254.1:n.338G=
ENST00000636930.2:c.4418G= MANE Select	ENSP00000490491.2:p.Gly1473=
ENST00000636940.1:n.2415G=
ENST00000637015.1:c.1786G=
ENST00000637568.1:c.1700G=
ENST00000637741.1:n.1084G=
ENST00000637810.1:c.1760G=	ENSP00000489636.1:p.Gly587=
ENST00000637904.1:c.1919G=	ENSP00000490550.1:p.Gly640=
ENST00000647938.1:c.4049G=	ENSP00000498155.1:p.Gly1350=
ENST00000346085.9:c.4049G=	ENSP00000344546.4:p.Gly1350=
ENST00000350026.9:c.4010G=	ENSP00000055163.7:p.Gly1337=
ENST00000414678.6:c.2576G=	ENSP00000412835.2:p.Gly859=
NM_017519.2:c.4010G=	NP_059989.2:p.Gly1337=
NM_020732.3:c.4049G=	NP_065783.3:p.Gly1350=
XM_005267069.3:c.4169G=	XP_005267126.2:p.Gly1390=
XM_011535984.1:c.3248G=	XP_011534286.1:p.Gly1083=
XM_011535985.1:c.3068G=	XP_011534287.1:p.Gly1023=
XM_011535986.1:c.2828G=	XP_011534288.1:p.Gly943=
XM_011535987.1:c.2447G=	XP_011534289.1:p.Gly816=
XM_011535988.1:c.1310G=	XP_011534290.1:p.Gly437=
NM_001346813.1:c.4169G=	NP_001333742.1:p.Gly1390=
NM_001363725.1:c.1919G=	NP_001350654.1:p.Gly640=
XM_011535984.2:c.4379G=	XP_011534286.2:p.Gly1460=
XM_011535988.3:c.1310G=	XP_011534290.1:p.Gly437=
XM_017011103.2:c.4280G=	XP_016866592.1:p.Gly1427=
XM_017011104.1:c.4250G=	XP_016866593.1:p.Gly1417=
XM_017011105.2:c.4220G=	XP_016866594.1:p.Gly1407=
XM_017011106.2:c.4091G=	XP_016866595.1:p.Gly1364=
XM_017011107.2:c.4070G=	XP_016866596.1:p.Gly1357=
XR_002956289.1:n.4427-1859G=
NM_001363725.2:c.1919G=	NP_001350654.1:p.Gly640=
NM_001371656.1:c.4298G=	NP_001358585.1:p.Gly1433=
NM_001374820.1:c.4298G=	NP_001361749.1:p.Gly1433=
NM_001374828.1:c.4418G= MANE Select	NP_001361757.1:p.Gly1473=
NM_017519.3:c.4259G=	NP_059989.3:p.Gly1420=