Canonical Allele Identifier: CA1675542191

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793912732

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198754del , CM000668.2:g.157198754del	GRCh38
NC_000006.11:g.157519888del , CM000668.1:g.157519888del	GRCh37
NC_000006.10:g.157561580del	NCBI36
NG_032093.1:g.425825del
NG_032093.2:g.425825del
NG_066624.1:g.427729del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4224-57del	ENSP00000055163.8:n.4224-57del
ENST00000414678.8:c.4293-57del	ENSP00000412835.3:n.4293-57del
ENST00000637015.2:c.4512-57del	ENSP00000489729.2:n.4512-57del
ENST00000346085.10:c.4263-57del	ENSP00000344546.5:n.4263-57del
ENST00000350026.10:c.3975-57del	ENSP00000055163.7:n.3975-57del
ENST00000414678.7:c.2541-57del	ENSP00000412835.2:n.2541-57del
ENST00000635849.1:c.1704-57del	ENSP00000490948.1:n.1704-57del
ENST00000635957.1:c.1335-57del	ENSP00000490385.1:n.1335-57del
ENST00000636227.1:n.2846-57del
ENST00000636254.1:n.246del
ENST00000636930.2:c.4383-57del MANE Select	ENSP00000490491.2:n.4383-57del
ENST00000636940.1:n.2380-57del
ENST00000637015.1:c.1751-57del
ENST00000637568.1:c.1665-57del
ENST00000637741.1:n.1049-57del
ENST00000637810.1:c.1725-57del	ENSP00000489636.1:n.1725-57del
ENST00000637904.1:c.1884-57del	ENSP00000490550.1:n.1884-57del
ENST00000647938.1:c.4014-57del	ENSP00000498155.1:n.4014-57del
ENST00000346085.9:c.4014-57del	ENSP00000344546.4:n.4014-57del
ENST00000350026.9:c.3975-57del	ENSP00000055163.7:n.3975-57del
ENST00000414678.6:c.2541-57del	ENSP00000412835.2:n.2541-57del
NM_017519.2:c.3975-57del	NP_059989.2:n.3975-57del
NM_020732.3:c.4014-57del	NP_065783.3:n.4014-57del
XM_005267069.3:c.4134-57del	XP_005267126.2:n.4134-57del
XM_011535984.1:c.3213-57del	XP_011534286.1:n.3213-57del
XM_011535985.1:c.3033-57del	XP_011534287.1:n.3033-57del
XM_011535986.1:c.2793-57del	XP_011534288.1:n.2793-57del
XM_011535987.1:c.2412-57del	XP_011534289.1:n.2412-57del
XM_011535988.1:c.1275-57del	XP_011534290.1:n.1275-57del
NM_001346813.1:c.4134-57del	NP_001333742.1:n.4134-57del
NM_001363725.1:c.1884-57del	NP_001350654.1:n.1884-57del
XM_011535984.2:c.4344-57del	XP_011534286.2:n.4344-57del
XM_011535988.3:c.1275-57del	XP_011534290.1:n.1275-57del
XM_017011103.2:c.4245-57del	XP_016866592.1:n.4245-57del
XM_017011104.1:c.4215-57del	XP_016866593.1:n.4215-57del
XM_017011105.2:c.4185-57del	XP_016866594.1:n.4185-57del
XM_017011106.2:c.4056-57del	XP_016866595.1:n.4056-57del
XM_017011107.2:c.4035-57del	XP_016866596.1:n.4035-57del
XR_002956289.1:n.4427-1951del
NM_001363725.2:c.1884-57del	NP_001350654.1:n.1884-57del
NM_001371656.1:c.4263-57del	NP_001358585.1:n.4263-57del
NM_001374820.1:c.4263-57del	NP_001361749.1:n.4263-57del
NM_001374828.1:c.4383-57del MANE Select	NP_001361757.1:n.4383-57del
NM_017519.3:c.4224-57del	NP_059989.3:n.4224-57del