Canonical Allele Identifier: CA2680915882

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157084819-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084825del , CM000668.2:g.157084825del	GRCh38
NC_000006.11:g.157405959del , CM000668.1:g.157405959del	GRCh37
NC_000006.10:g.157447651del	NCBI36
NG_032093.1:g.311896del
NG_032093.2:g.311896del
NG_066624.1:g.313800del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2411del	ENSP00000055163.8:p.Gly804AlafsTer11
ENST00000414678.8:c.2411del	ENSP00000412835.3:p.Gly804AlafsTer11
ENST00000637015.2:c.2411del	ENSP00000489729.2:p.Gly804AlafsTer11
ENST00000319584.11:c.425del	ENSP00000313006.7:p.Gly142AlafsTer11
ENST00000346085.10:c.2450del	ENSP00000344546.5:p.Gly817AlafsTer11
ENST00000350026.10:c.2162del	ENSP00000055163.7:p.Gly721AlafsTer11
ENST00000414678.7:c.659del	ENSP00000412835.2:p.Gly220AlafsTer11
ENST00000452544.2:n.312del
ENST00000493658.2:n.60del
ENST00000635849.1:c.-89del	ENSP00000490948.1:n.-89del
ENST00000636930.2:c.2411del MANE Select	ENSP00000490491.2:p.Gly804AlafsTer11
ENST00000637003.1:c.-89del	ENSP00000489666.1:n.-89del
ENST00000637810.1:c.-89del	ENSP00000489636.1:n.-89del
ENST00000637904.1:c.-89del	ENSP00000490550.1:n.-89del
ENST00000647938.1:c.2201del	ENSP00000498155.1:p.Gly734AlafsTer11
ENST00000674190.1:n.1160del
ENST00000319584.10:c.428del	ENSP00000313006.6:p.Gly143AlafsTer11
ENST00000346085.9:c.2201del	ENSP00000344546.4:p.Gly734AlafsTer11
ENST00000350026.9:c.2162del	ENSP00000055163.7:p.Gly721AlafsTer11
ENST00000414678.6:c.659del	ENSP00000412835.2:p.Gly220AlafsTer11
ENST00000452544.1:n.270del
ENST00000493658.1:n.60del
NM_017519.2:c.2162del	NP_059989.2:p.Gly721AlafsTer11
NM_020732.3:c.2201del	NP_065783.3:p.Gly734AlafsTer11
XM_005267069.3:c.2162del	XP_005267126.2:p.Gly721AlafsTer11
XM_011535984.1:c.1112del	XP_011534286.1:p.Gly371AlafsTer11
XM_011535985.1:c.1112del	XP_011534287.1:p.Gly371AlafsTer11
XM_011535986.1:c.692del	XP_011534288.1:p.Gly231AlafsTer11
XM_011535987.1:c.311del	XP_011534289.1:p.Gly104AlafsTer11
NM_001346813.1:c.2162del	NP_001333742.1:p.Gly721AlafsTer11
NM_001363725.1:c.-89del	NP_001350654.1:n.-89del
XM_011535984.2:c.2243del	XP_011534286.2:p.Gly748AlafsTer11
XM_017011103.2:c.2243del	XP_016866592.1:p.Gly748AlafsTer11
XM_017011104.1:c.2243del	XP_016866593.1:p.Gly748AlafsTer11
XM_017011105.2:c.2243del	XP_016866594.1:p.Gly748AlafsTer11
XM_017011106.2:c.2243del	XP_016866595.1:p.Gly748AlafsTer11
XM_017011107.2:c.2243del	XP_016866596.1:p.Gly748AlafsTer11
XR_002956289.1:n.2326del
NM_001363725.2:c.-89del	NP_001350654.1:n.-89del
NM_001371656.1:c.2450del	NP_001358585.1:p.Gly817AlafsTer11
NM_001374820.1:c.2450del	NP_001361749.1:p.Gly817AlafsTer11
NM_001374828.1:c.2411del MANE Select	NP_001361757.1:p.Gly804AlafsTer11
NM_017519.3:c.2411del	NP_059989.3:p.Gly804AlafsTer11