Canonical Allele Identifier: CA366241517

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522151T>G (hg19) ; chr6:g.157201017T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201017T>G , CM000668.2:g.157201017T>G	GRCh38
NC_000006.11:g.157522151T>G , CM000668.1:g.157522151T>G	GRCh37
NC_000006.10:g.157563843T>G	NCBI36
NG_032093.1:g.428088T>G
NG_032093.2:g.428088T>G
NG_066624.1:g.429992T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4633T>G	ENSP00000055163.8:p.Tyr1545Asp
ENST00000414678.8:c.4702T>G	ENSP00000412835.3:p.Tyr1568Asp
ENST00000637015.2:c.4921T>G	ENSP00000489729.2:p.Tyr1641Asp
ENST00000346085.10:c.4672T>G	ENSP00000344546.5:p.Tyr1558Asp
ENST00000350026.10:c.4384T>G	ENSP00000055163.7:p.Tyr1462Asp
ENST00000414678.7:c.2950T>G	ENSP00000412835.2:p.Tyr984Asp
ENST00000635849.1:c.2113T>G	ENSP00000490948.1:p.Tyr705Asp
ENST00000635957.1:c.1744T>G	ENSP00000490385.1:p.Tyr582Asp
ENST00000636227.1:n.3255T>G
ENST00000636254.1:n.712T>G
ENST00000636930.2:c.4792T>G MANE Select	ENSP00000490491.2:p.Tyr1598Asp
ENST00000636940.1:n.2789T>G
ENST00000637015.1:c.2160T>G
ENST00000637568.1:c.2074T>G
ENST00000637741.1:n.1458T>G
ENST00000637810.1:c.2134T>G	ENSP00000489636.1:p.Tyr712Asp
ENST00000637904.1:c.2293T>G	ENSP00000490550.1:p.Tyr765Asp
ENST00000647938.1:c.4423T>G	ENSP00000498155.1:p.Tyr1475Asp
ENST00000346085.9:c.4423T>G	ENSP00000344546.4:p.Tyr1475Asp
ENST00000350026.9:c.4384T>G	ENSP00000055163.7:p.Tyr1462Asp
ENST00000414678.6:c.2950T>G	ENSP00000412835.2:p.Tyr984Asp
NM_017519.2:c.4384T>G	NP_059989.2:p.Tyr1462Asp
NM_020732.3:c.4423T>G	NP_065783.3:p.Tyr1475Asp
XM_005267069.3:c.4543T>G	XP_005267126.2:p.Tyr1515Asp
XM_011535984.1:c.3622T>G	XP_011534286.1:p.Tyr1208Asp
XM_011535985.1:c.3442T>G	XP_011534287.1:p.Tyr1148Asp
XM_011535986.1:c.3202T>G	XP_011534288.1:p.Tyr1068Asp
XM_011535987.1:c.2821T>G	XP_011534289.1:p.Tyr941Asp
XM_011535988.1:c.1684T>G	XP_011534290.1:p.Tyr562Asp
NM_001346813.1:c.4543T>G	NP_001333742.1:p.Tyr1515Asp
NM_001363725.1:c.2293T>G	NP_001350654.1:p.Tyr765Asp
XM_011535984.2:c.4753T>G	XP_011534286.2:p.Tyr1585Asp
XM_011535988.3:c.1684T>G	XP_011534290.1:p.Tyr562Asp
XM_017011103.2:c.4654T>G	XP_016866592.1:p.Tyr1552Asp
XM_017011104.1:c.4624T>G	XP_016866593.1:p.Tyr1542Asp
XM_017011105.2:c.4594T>G	XP_016866594.1:p.Tyr1532Asp
XM_017011106.2:c.4465T>G	XP_016866595.1:p.Tyr1489Asp
XM_017011107.2:c.4444T>G	XP_016866596.1:p.Tyr1482Asp
XR_002956289.1:n.4739T>G
NM_001363725.2:c.2293T>G	NP_001350654.1:p.Tyr765Asp
NM_001371656.1:c.4672T>G	NP_001358585.1:p.Tyr1558Asp
NM_001374820.1:c.4672T>G	NP_001361749.1:p.Tyr1558Asp
NM_001374828.1:c.4792T>G MANE Select	NP_001361757.1:p.Tyr1598Asp
NM_017519.3:c.4633T>G	NP_059989.3:p.Tyr1545Asp