Canonical Allele Identifier: CA366241780

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 521539
• ClinVar RCV Id: RCV000622809
• dbSNP Id: rs1554235792
• MyVariant Identifiers: chr6:g.157522198C>G (hg19) ; chr6:g.157201064C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201064C>G , CM000668.2:g.157201064C>G	GRCh38
NC_000006.11:g.157522198C>G , CM000668.1:g.157522198C>G	GRCh37
NC_000006.10:g.157563890C>G	NCBI36
NG_032093.1:g.428135C>G
NG_032093.2:g.428135C>G
NG_066624.1:g.430039C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4680C>G	ENSP00000055163.8:p.Tyr1560Ter
ENST00000414678.8:c.4749C>G	ENSP00000412835.3:p.Tyr1583Ter
ENST00000637015.2:c.4968C>G	ENSP00000489729.2:p.Tyr1656Ter
ENST00000346085.10:c.4719C>G	ENSP00000344546.5:p.Tyr1573Ter
ENST00000350026.10:c.4431C>G	ENSP00000055163.7:p.Tyr1477Ter
ENST00000414678.7:c.2997C>G	ENSP00000412835.2:p.Tyr999Ter
ENST00000635849.1:c.2160C>G	ENSP00000490948.1:p.Tyr720Ter
ENST00000635957.1:c.1791C>G	ENSP00000490385.1:p.Tyr597Ter
ENST00000636227.1:n.3302C>G
ENST00000636254.1:n.759C>G
ENST00000636930.2:c.4839C>G MANE Select	ENSP00000490491.2:p.Tyr1613Ter
ENST00000636940.1:n.2836C>G
ENST00000637015.1:c.2207C>G
ENST00000637568.1:c.2121C>G
ENST00000637741.1:n.1505C>G
ENST00000637810.1:c.2181C>G	ENSP00000489636.1:p.Tyr727Ter
ENST00000637904.1:c.2340C>G	ENSP00000490550.1:p.Tyr780Ter
ENST00000647938.1:c.4470C>G	ENSP00000498155.1:p.Tyr1490Ter
ENST00000346085.9:c.4470C>G	ENSP00000344546.4:p.Tyr1490Ter
ENST00000350026.9:c.4431C>G	ENSP00000055163.7:p.Tyr1477Ter
ENST00000414678.6:c.2997C>G	ENSP00000412835.2:p.Tyr999Ter
NM_017519.2:c.4431C>G	NP_059989.2:p.Tyr1477Ter
NM_020732.3:c.4470C>G	NP_065783.3:p.Tyr1490Ter
XM_005267069.3:c.4590C>G	XP_005267126.2:p.Tyr1530Ter
XM_011535984.1:c.3669C>G	XP_011534286.1:p.Tyr1223Ter
XM_011535985.1:c.3489C>G	XP_011534287.1:p.Tyr1163Ter
XM_011535986.1:c.3249C>G	XP_011534288.1:p.Tyr1083Ter
XM_011535987.1:c.2868C>G	XP_011534289.1:p.Tyr956Ter
XM_011535988.1:c.1731C>G	XP_011534290.1:p.Tyr577Ter
NM_001346813.1:c.4590C>G	NP_001333742.1:p.Tyr1530Ter
NM_001363725.1:c.2340C>G	NP_001350654.1:p.Tyr780Ter
XM_011535984.2:c.4800C>G	XP_011534286.2:p.Tyr1600Ter
XM_011535988.3:c.1731C>G	XP_011534290.1:p.Tyr577Ter
XM_017011103.2:c.4701C>G	XP_016866592.1:p.Tyr1567Ter
XM_017011104.1:c.4671C>G	XP_016866593.1:p.Tyr1557Ter
XM_017011105.2:c.4641C>G	XP_016866594.1:p.Tyr1547Ter
XM_017011106.2:c.4512C>G	XP_016866595.1:p.Tyr1504Ter
XM_017011107.2:c.4491C>G	XP_016866596.1:p.Tyr1497Ter
XR_002956289.1:n.4786C>G
NM_001363725.2:c.2340C>G	NP_001350654.1:p.Tyr780Ter
NM_001371656.1:c.4719C>G	NP_001358585.1:p.Tyr1573Ter
NM_001374820.1:c.4719C>G	NP_001361749.1:p.Tyr1573Ter
NM_001374828.1:c.4839C>G MANE Select	NP_001361757.1:p.Tyr1613Ter
NM_017519.3:c.4680C>G	NP_059989.3:p.Tyr1560Ter