Canonical Allele Identifier: CA821316243

Gene: ARID1B

Linked Data

• dbSNP Id: rs1369675196
• gnomAD v3: 6-157199122-CAT-C
• gnomAD v4: 6-157199122-CAT-C
• MyVariant Identifiers: chr6:g.157520257_157520258del (hg19) ; chr6:g.157199123_157199124del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199125_157199126del , CM000668.2:g.157199125_157199126del	GRCh38
NC_000006.11:g.157520259_157520260del , CM000668.1:g.157520259_157520260del	GRCh37
NC_000006.10:g.157561951_157561952del	NCBI36
NG_032093.1:g.426196_426197del
NG_032093.2:g.426196_426197del
NG_066624.1:g.428100_428101del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+218_4320+219del	ENSP00000055163.8:n.4320+218_4320+219del
ENST00000414678.8:c.4389+218_4389+219del	ENSP00000412835.3:n.4389+218_4389+219del
ENST00000637015.2:c.4608+218_4608+219del	ENSP00000489729.2:n.4608+218_4608+219del
ENST00000346085.10:c.4359+218_4359+219del	ENSP00000344546.5:n.4359+218_4359+219del
ENST00000350026.10:c.4071+218_4071+219del	ENSP00000055163.7:n.4071+218_4071+219del
ENST00000414678.7:c.2637+218_2637+219del	ENSP00000412835.2:n.2637+218_2637+219del
ENST00000635849.1:c.1800+218_1800+219del	ENSP00000490948.1:n.1800+218_1800+219del
ENST00000635957.1:c.1431+218_1431+219del	ENSP00000490385.1:n.1431+218_1431+219del
ENST00000636227.1:n.2942+218_2942+219del
ENST00000636254.1:n.399+218_399+219del
ENST00000636930.2:c.4479+218_4479+219del MANE Select	ENSP00000490491.2:n.4479+218_4479+219del
ENST00000636940.1:n.2476+218_2476+219del
ENST00000637015.1:c.1847+218_1847+219del
ENST00000637568.1:c.1761+218_1761+219del
ENST00000637741.1:n.1145+218_1145+219del
ENST00000637810.1:c.1821+218_1821+219del	ENSP00000489636.1:n.1821+218_1821+219del
ENST00000637904.1:c.1980+218_1980+219del	ENSP00000490550.1:n.1980+218_1980+219del
ENST00000647938.1:c.4110+218_4110+219del	ENSP00000498155.1:n.4110+218_4110+219del
ENST00000346085.9:c.4110+218_4110+219del	ENSP00000344546.4:n.4110+218_4110+219del
ENST00000350026.9:c.4071+218_4071+219del	ENSP00000055163.7:n.4071+218_4071+219del
ENST00000414678.6:c.2637+218_2637+219del	ENSP00000412835.2:n.2637+218_2637+219del
NM_017519.2:c.4071+218_4071+219del	NP_059989.2:n.4071+218_4071+219del
NM_020732.3:c.4110+218_4110+219del	NP_065783.3:n.4110+218_4110+219del
XM_005267069.3:c.4230+218_4230+219del	XP_005267126.2:n.4230+218_4230+219del
XM_011535984.1:c.3309+218_3309+219del	XP_011534286.1:n.3309+218_3309+219del
XM_011535985.1:c.3129+218_3129+219del	XP_011534287.1:n.3129+218_3129+219del
XM_011535986.1:c.2889+218_2889+219del	XP_011534288.1:n.2889+218_2889+219del
XM_011535987.1:c.2508+218_2508+219del	XP_011534289.1:n.2508+218_2508+219del
XM_011535988.1:c.1371+218_1371+219del	XP_011534290.1:n.1371+218_1371+219del
NM_001346813.1:c.4230+218_4230+219del	NP_001333742.1:n.4230+218_4230+219del
NM_001363725.1:c.1980+218_1980+219del	NP_001350654.1:n.1980+218_1980+219del
XM_011535984.2:c.4440+218_4440+219del	XP_011534286.2:n.4440+218_4440+219del
XM_011535988.3:c.1371+218_1371+219del	XP_011534290.1:n.1371+218_1371+219del
XM_017011103.2:c.4341+218_4341+219del	XP_016866592.1:n.4341+218_4341+219del
XM_017011104.1:c.4311+218_4311+219del	XP_016866593.1:n.4311+218_4311+219del
XM_017011105.2:c.4281+218_4281+219del	XP_016866594.1:n.4281+218_4281+219del
XM_017011106.2:c.4152+218_4152+219del	XP_016866595.1:n.4152+218_4152+219del
XM_017011107.2:c.4131+218_4131+219del	XP_016866596.1:n.4131+218_4131+219del
XR_002956289.1:n.4427-1580_4427-1579del
NM_001363725.2:c.1980+218_1980+219del	NP_001350654.1:n.1980+218_1980+219del
NM_001371656.1:c.4359+218_4359+219del	NP_001358585.1:n.4359+218_4359+219del
NM_001374820.1:c.4359+218_4359+219del	NP_001361749.1:n.4359+218_4359+219del
NM_001374828.1:c.4479+218_4479+219del MANE Select	NP_001361757.1:n.4479+218_4479+219del
NM_017519.3:c.4320+218_4320+219del	NP_059989.3:n.4320+218_4320+219del