Canonical Allele Identifier: CA366240920

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200782C>A , CM000668.2:g.157200782C>A	GRCh38
NC_000006.11:g.157521916C>A , CM000668.1:g.157521916C>A	GRCh37
NC_000006.10:g.157563608C>A	NCBI36
NG_032093.1:g.427853C>A
NG_032093.2:g.427853C>A
NG_066624.1:g.429757C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4398C>A	ENSP00000055163.8:p.Tyr1466Ter
ENST00000414678.8:c.4467C>A	ENSP00000412835.3:p.Tyr1489Ter
ENST00000637015.2:c.4686C>A	ENSP00000489729.2:p.Tyr1562Ter
ENST00000346085.10:c.4437C>A	ENSP00000344546.5:p.Tyr1479Ter
ENST00000350026.10:c.4149C>A	ENSP00000055163.7:p.Tyr1383Ter
ENST00000414678.7:c.2715C>A	ENSP00000412835.2:p.Tyr905Ter
ENST00000635849.1:c.1878C>A	ENSP00000490948.1:p.Tyr626Ter
ENST00000635957.1:c.1509C>A	ENSP00000490385.1:p.Tyr503Ter
ENST00000636227.1:n.3020C>A
ENST00000636254.1:n.477C>A
ENST00000636930.2:c.4557C>A MANE Select	ENSP00000490491.2:p.Tyr1519Ter
ENST00000636940.1:n.2554C>A
ENST00000637015.1:c.1925C>A
ENST00000637568.1:c.1839C>A
ENST00000637741.1:n.1223C>A
ENST00000637810.1:c.1899C>A	ENSP00000489636.1:p.Tyr633Ter
ENST00000637904.1:c.2058C>A	ENSP00000490550.1:p.Tyr686Ter
ENST00000647938.1:c.4188C>A	ENSP00000498155.1:p.Tyr1396Ter
ENST00000346085.9:c.4188C>A	ENSP00000344546.4:p.Tyr1396Ter
ENST00000350026.9:c.4149C>A	ENSP00000055163.7:p.Tyr1383Ter
ENST00000414678.6:c.2715C>A	ENSP00000412835.2:p.Tyr905Ter
NM_017519.2:c.4149C>A	NP_059989.2:p.Tyr1383Ter
NM_020732.3:c.4188C>A	NP_065783.3:p.Tyr1396Ter
XM_005267069.3:c.4308C>A	XP_005267126.2:p.Tyr1436Ter
XM_011535984.1:c.3387C>A	XP_011534286.1:p.Tyr1129Ter
XM_011535985.1:c.3207C>A	XP_011534287.1:p.Tyr1069Ter
XM_011535986.1:c.2967C>A	XP_011534288.1:p.Tyr989Ter
XM_011535987.1:c.2586C>A	XP_011534289.1:p.Tyr862Ter
XM_011535988.1:c.1449C>A	XP_011534290.1:p.Tyr483Ter
NM_001346813.1:c.4308C>A	NP_001333742.1:p.Tyr1436Ter
NM_001363725.1:c.2058C>A	NP_001350654.1:p.Tyr686Ter
XM_011535984.2:c.4518C>A	XP_011534286.2:p.Tyr1506Ter
XM_011535988.3:c.1449C>A	XP_011534290.1:p.Tyr483Ter
XM_017011103.2:c.4419C>A	XP_016866592.1:p.Tyr1473Ter
XM_017011104.1:c.4389C>A	XP_016866593.1:p.Tyr1463Ter
XM_017011105.2:c.4359C>A	XP_016866594.1:p.Tyr1453Ter
XM_017011106.2:c.4230C>A	XP_016866595.1:p.Tyr1410Ter
XM_017011107.2:c.4209C>A	XP_016866596.1:p.Tyr1403Ter
XR_002956289.1:n.4504C>A
NM_001363725.2:c.2058C>A	NP_001350654.1:p.Tyr686Ter
NM_001371656.1:c.4437C>A	NP_001358585.1:p.Tyr1479Ter
NM_001374820.1:c.4437C>A	NP_001361749.1:p.Tyr1479Ter
NM_001374828.1:c.4557C>A MANE Select	NP_001361757.1:p.Tyr1519Ter
NM_017519.3:c.4398C>A	NP_059989.3:p.Tyr1466Ter