Canonical Allele Identifier: CA366241529

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1212586
• ClinVar RCV Id: RCV001586233
• dbSNP Id: rs1562345819
• MyVariant Identifiers: chr6:g.157522153C>A (hg19) ; chr6:g.157201019C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201019C>A , CM000668.2:g.157201019C>A	GRCh38
NC_000006.11:g.157522153C>A , CM000668.1:g.157522153C>A	GRCh37
NC_000006.10:g.157563845C>A	NCBI36
NG_032093.1:g.428090C>A
NG_032093.2:g.428090C>A
NG_066624.1:g.429994C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4635C>A	ENSP00000055163.8:p.Tyr1545Ter
ENST00000414678.8:c.4704C>A	ENSP00000412835.3:p.Tyr1568Ter
ENST00000637015.2:c.4923C>A	ENSP00000489729.2:p.Tyr1641Ter
ENST00000346085.10:c.4674C>A	ENSP00000344546.5:p.Tyr1558Ter
ENST00000350026.10:c.4386C>A	ENSP00000055163.7:p.Tyr1462Ter
ENST00000414678.7:c.2952C>A	ENSP00000412835.2:p.Tyr984Ter
ENST00000635849.1:c.2115C>A	ENSP00000490948.1:p.Tyr705Ter
ENST00000635957.1:c.1746C>A	ENSP00000490385.1:p.Tyr582Ter
ENST00000636227.1:n.3257C>A
ENST00000636254.1:n.714C>A
ENST00000636930.2:c.4794C>A MANE Select	ENSP00000490491.2:p.Tyr1598Ter
ENST00000636940.1:n.2791C>A
ENST00000637015.1:c.2162C>A
ENST00000637568.1:c.2076C>A
ENST00000637741.1:n.1460C>A
ENST00000637810.1:c.2136C>A	ENSP00000489636.1:p.Tyr712Ter
ENST00000637904.1:c.2295C>A	ENSP00000490550.1:p.Tyr765Ter
ENST00000647938.1:c.4425C>A	ENSP00000498155.1:p.Tyr1475Ter
ENST00000346085.9:c.4425C>A	ENSP00000344546.4:p.Tyr1475Ter
ENST00000350026.9:c.4386C>A	ENSP00000055163.7:p.Tyr1462Ter
ENST00000414678.6:c.2952C>A	ENSP00000412835.2:p.Tyr984Ter
NM_017519.2:c.4386C>A	NP_059989.2:p.Tyr1462Ter
NM_020732.3:c.4425C>A	NP_065783.3:p.Tyr1475Ter
XM_005267069.3:c.4545C>A	XP_005267126.2:p.Tyr1515Ter
XM_011535984.1:c.3624C>A	XP_011534286.1:p.Tyr1208Ter
XM_011535985.1:c.3444C>A	XP_011534287.1:p.Tyr1148Ter
XM_011535986.1:c.3204C>A	XP_011534288.1:p.Tyr1068Ter
XM_011535987.1:c.2823C>A	XP_011534289.1:p.Tyr941Ter
XM_011535988.1:c.1686C>A	XP_011534290.1:p.Tyr562Ter
NM_001346813.1:c.4545C>A	NP_001333742.1:p.Tyr1515Ter
NM_001363725.1:c.2295C>A	NP_001350654.1:p.Tyr765Ter
XM_011535984.2:c.4755C>A	XP_011534286.2:p.Tyr1585Ter
XM_011535988.3:c.1686C>A	XP_011534290.1:p.Tyr562Ter
XM_017011103.2:c.4656C>A	XP_016866592.1:p.Tyr1552Ter
XM_017011104.1:c.4626C>A	XP_016866593.1:p.Tyr1542Ter
XM_017011105.2:c.4596C>A	XP_016866594.1:p.Tyr1532Ter
XM_017011106.2:c.4467C>A	XP_016866595.1:p.Tyr1489Ter
XM_017011107.2:c.4446C>A	XP_016866596.1:p.Tyr1482Ter
XR_002956289.1:n.4741C>A
NM_001363725.2:c.2295C>A	NP_001350654.1:p.Tyr765Ter
NM_001371656.1:c.4674C>A	NP_001358585.1:p.Tyr1558Ter
NM_001374820.1:c.4674C>A	NP_001361749.1:p.Tyr1558Ter
NM_001374828.1:c.4794C>A MANE Select	NP_001361757.1:p.Tyr1598Ter
NM_017519.3:c.4635C>A	NP_059989.3:p.Tyr1545Ter