Canonical Allele Identifier: CA2680895529

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157199021-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199024del , CM000668.2:g.157199024del	GRCh38
NC_000006.11:g.157520158del , CM000668.1:g.157520158del	GRCh37
NC_000006.10:g.157561850del	NCBI36
NG_032093.1:g.426095del
NG_032093.2:g.426095del
NG_066624.1:g.427999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+117del	ENSP00000055163.8:n.4320+117del
ENST00000414678.8:c.4389+117del	ENSP00000412835.3:n.4389+117del
ENST00000637015.2:c.4608+117del	ENSP00000489729.2:n.4608+117del
ENST00000346085.10:c.4359+117del	ENSP00000344546.5:n.4359+117del
ENST00000350026.10:c.4071+117del	ENSP00000055163.7:n.4071+117del
ENST00000414678.7:c.2637+117del	ENSP00000412835.2:n.2637+117del
ENST00000635849.1:c.1800+117del	ENSP00000490948.1:n.1800+117del
ENST00000635957.1:c.1431+117del	ENSP00000490385.1:n.1431+117del
ENST00000636227.1:n.2942+117del
ENST00000636254.1:n.399+117del
ENST00000636930.2:c.4479+117del MANE Select	ENSP00000490491.2:n.4479+117del
ENST00000636940.1:n.2476+117del
ENST00000637015.1:c.1847+117del
ENST00000637568.1:c.1761+117del
ENST00000637741.1:n.1145+117del
ENST00000637810.1:c.1821+117del	ENSP00000489636.1:n.1821+117del
ENST00000637904.1:c.1980+117del	ENSP00000490550.1:n.1980+117del
ENST00000647938.1:c.4110+117del	ENSP00000498155.1:n.4110+117del
ENST00000346085.9:c.4110+117del	ENSP00000344546.4:n.4110+117del
ENST00000350026.9:c.4071+117del	ENSP00000055163.7:n.4071+117del
ENST00000414678.6:c.2637+117del	ENSP00000412835.2:n.2637+117del
NM_017519.2:c.4071+117del	NP_059989.2:n.4071+117del
NM_020732.3:c.4110+117del	NP_065783.3:n.4110+117del
XM_005267069.3:c.4230+117del	XP_005267126.2:n.4230+117del
XM_011535984.1:c.3309+117del	XP_011534286.1:n.3309+117del
XM_011535985.1:c.3129+117del	XP_011534287.1:n.3129+117del
XM_011535986.1:c.2889+117del	XP_011534288.1:n.2889+117del
XM_011535987.1:c.2508+117del	XP_011534289.1:n.2508+117del
XM_011535988.1:c.1371+117del	XP_011534290.1:n.1371+117del
NM_001346813.1:c.4230+117del	NP_001333742.1:n.4230+117del
NM_001363725.1:c.1980+117del	NP_001350654.1:n.1980+117del
XM_011535984.2:c.4440+117del	XP_011534286.2:n.4440+117del
XM_011535988.3:c.1371+117del	XP_011534290.1:n.1371+117del
XM_017011103.2:c.4341+117del	XP_016866592.1:n.4341+117del
XM_017011104.1:c.4311+117del	XP_016866593.1:n.4311+117del
XM_017011105.2:c.4281+117del	XP_016866594.1:n.4281+117del
XM_017011106.2:c.4152+117del	XP_016866595.1:n.4152+117del
XM_017011107.2:c.4131+117del	XP_016866596.1:n.4131+117del
XR_002956289.1:n.4427-1681del
NM_001363725.2:c.1980+117del	NP_001350654.1:n.1980+117del
NM_001371656.1:c.4359+117del	NP_001358585.1:n.4359+117del
NM_001374820.1:c.4359+117del	NP_001361749.1:n.4359+117del
NM_001374828.1:c.4479+117del MANE Select	NP_001361757.1:n.4479+117del
NM_017519.3:c.4320+117del	NP_059989.3:n.4320+117del