Canonical Allele Identifier: CA366242137

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201159-A-G
• MyVariant Identifiers: chr6:g.157522293A>G (hg19) ; chr6:g.157201159A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201159A>G , CM000668.2:g.157201159A>G	GRCh38
NC_000006.11:g.157522293A>G , CM000668.1:g.157522293A>G	GRCh37
NC_000006.10:g.157563985A>G	NCBI36
NG_032093.1:g.428230A>G
NG_032093.2:g.428230A>G
NG_066624.1:g.430134A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4775A>G	ENSP00000055163.8:p.Tyr1592Cys
ENST00000414678.8:c.4844A>G	ENSP00000412835.3:p.Tyr1615Cys
ENST00000637015.2:c.5063A>G	ENSP00000489729.2:p.Tyr1688Cys
ENST00000346085.10:c.4814A>G	ENSP00000344546.5:p.Tyr1605Cys
ENST00000350026.10:c.4526A>G	ENSP00000055163.7:p.Tyr1509Cys
ENST00000414678.7:c.3092A>G	ENSP00000412835.2:p.Tyr1031Cys
ENST00000635849.1:c.2255A>G	ENSP00000490948.1:p.Tyr752Cys
ENST00000635957.1:c.1886A>G	ENSP00000490385.1:p.Tyr629Cys
ENST00000636227.1:n.3397A>G
ENST00000636254.1:n.854A>G
ENST00000636930.2:c.4934A>G MANE Select	ENSP00000490491.2:p.Tyr1645Cys
ENST00000636940.1:n.2931A>G
ENST00000637015.1:c.2302A>G
ENST00000637568.1:c.2216A>G
ENST00000637741.1:n.1600A>G
ENST00000637810.1:c.2276A>G	ENSP00000489636.1:p.Tyr759Cys
ENST00000637904.1:c.2435A>G	ENSP00000490550.1:p.Tyr812Cys
ENST00000647938.1:c.4565A>G	ENSP00000498155.1:p.Tyr1522Cys
ENST00000346085.9:c.4565A>G	ENSP00000344546.4:p.Tyr1522Cys
ENST00000350026.9:c.4526A>G	ENSP00000055163.7:p.Tyr1509Cys
ENST00000414678.6:c.3092A>G	ENSP00000412835.2:p.Tyr1031Cys
NM_017519.2:c.4526A>G	NP_059989.2:p.Tyr1509Cys
NM_020732.3:c.4565A>G	NP_065783.3:p.Tyr1522Cys
XM_005267069.3:c.4685A>G	XP_005267126.2:p.Tyr1562Cys
XM_011535984.1:c.3764A>G	XP_011534286.1:p.Tyr1255Cys
XM_011535985.1:c.3584A>G	XP_011534287.1:p.Tyr1195Cys
XM_011535986.1:c.3344A>G	XP_011534288.1:p.Tyr1115Cys
XM_011535987.1:c.2963A>G	XP_011534289.1:p.Tyr988Cys
XM_011535988.1:c.1826A>G	XP_011534290.1:p.Tyr609Cys
NM_001346813.1:c.4685A>G	NP_001333742.1:p.Tyr1562Cys
NM_001363725.1:c.2435A>G	NP_001350654.1:p.Tyr812Cys
XM_011535984.2:c.4895A>G	XP_011534286.2:p.Tyr1632Cys
XM_011535988.3:c.1826A>G	XP_011534290.1:p.Tyr609Cys
XM_017011103.2:c.4796A>G	XP_016866592.1:p.Tyr1599Cys
XM_017011104.1:c.4766A>G	XP_016866593.1:p.Tyr1589Cys
XM_017011105.2:c.4736A>G	XP_016866594.1:p.Tyr1579Cys
XM_017011106.2:c.4607A>G	XP_016866595.1:p.Tyr1536Cys
XM_017011107.2:c.4586A>G	XP_016866596.1:p.Tyr1529Cys
XR_002956289.1:n.4881A>G
NM_001363725.2:c.2435A>G	NP_001350654.1:p.Tyr812Cys
NM_001371656.1:c.4814A>G	NP_001358585.1:p.Tyr1605Cys
NM_001374820.1:c.4814A>G	NP_001361749.1:p.Tyr1605Cys
NM_001374828.1:c.4934A>G MANE Select	NP_001361757.1:p.Tyr1645Cys
NM_017519.3:c.4775A>G	NP_059989.3:p.Tyr1592Cys