Canonical Allele Identifier: CA366240962

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200798G>A , CM000668.2:g.157200798G>A	GRCh38
NC_000006.11:g.157521932G>A , CM000668.1:g.157521932G>A	GRCh37
NC_000006.10:g.157563624G>A	NCBI36
NG_032093.1:g.427869G>A
NG_032093.2:g.427869G>A
NG_066624.1:g.429773G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4414G>A	ENSP00000055163.8:p.Glu1472Lys
ENST00000414678.8:c.4483G>A	ENSP00000412835.3:p.Glu1495Lys
ENST00000637015.2:c.4702G>A	ENSP00000489729.2:p.Glu1568Lys
ENST00000346085.10:c.4453G>A	ENSP00000344546.5:p.Glu1485Lys
ENST00000350026.10:c.4165G>A	ENSP00000055163.7:p.Glu1389Lys
ENST00000414678.7:c.2731G>A	ENSP00000412835.2:p.Glu911Lys
ENST00000635849.1:c.1894G>A	ENSP00000490948.1:p.Glu632Lys
ENST00000635957.1:c.1525G>A	ENSP00000490385.1:p.Glu509Lys
ENST00000636227.1:n.3036G>A
ENST00000636254.1:n.493G>A
ENST00000636930.2:c.4573G>A MANE Select	ENSP00000490491.2:p.Glu1525Lys
ENST00000636940.1:n.2570G>A
ENST00000637015.1:c.1941G>A
ENST00000637568.1:c.1855G>A
ENST00000637741.1:n.1239G>A
ENST00000637810.1:c.1915G>A	ENSP00000489636.1:p.Glu639Lys
ENST00000637904.1:c.2074G>A	ENSP00000490550.1:p.Glu692Lys
ENST00000647938.1:c.4204G>A	ENSP00000498155.1:p.Glu1402Lys
ENST00000346085.9:c.4204G>A	ENSP00000344546.4:p.Glu1402Lys
ENST00000350026.9:c.4165G>A	ENSP00000055163.7:p.Glu1389Lys
ENST00000414678.6:c.2731G>A	ENSP00000412835.2:p.Glu911Lys
NM_017519.2:c.4165G>A	NP_059989.2:p.Glu1389Lys
NM_020732.3:c.4204G>A	NP_065783.3:p.Glu1402Lys
XM_005267069.3:c.4324G>A	XP_005267126.2:p.Glu1442Lys
XM_011535984.1:c.3403G>A	XP_011534286.1:p.Glu1135Lys
XM_011535985.1:c.3223G>A	XP_011534287.1:p.Glu1075Lys
XM_011535986.1:c.2983G>A	XP_011534288.1:p.Glu995Lys
XM_011535987.1:c.2602G>A	XP_011534289.1:p.Glu868Lys
XM_011535988.1:c.1465G>A	XP_011534290.1:p.Glu489Lys
NM_001346813.1:c.4324G>A	NP_001333742.1:p.Glu1442Lys
NM_001363725.1:c.2074G>A	NP_001350654.1:p.Glu692Lys
XM_011535984.2:c.4534G>A	XP_011534286.2:p.Glu1512Lys
XM_011535988.3:c.1465G>A	XP_011534290.1:p.Glu489Lys
XM_017011103.2:c.4435G>A	XP_016866592.1:p.Glu1479Lys
XM_017011104.1:c.4405G>A	XP_016866593.1:p.Glu1469Lys
XM_017011105.2:c.4375G>A	XP_016866594.1:p.Glu1459Lys
XM_017011106.2:c.4246G>A	XP_016866595.1:p.Glu1416Lys
XM_017011107.2:c.4225G>A	XP_016866596.1:p.Glu1409Lys
XR_002956289.1:n.4520G>A
NM_001363725.2:c.2074G>A	NP_001350654.1:p.Glu692Lys
NM_001371656.1:c.4453G>A	NP_001358585.1:p.Glu1485Lys
NM_001374820.1:c.4453G>A	NP_001361749.1:p.Glu1485Lys
NM_001374828.1:c.4573G>A MANE Select	NP_001361757.1:p.Glu1525Lys
NM_017519.3:c.4414G>A	NP_059989.3:p.Glu1472Lys