Canonical Allele Identifier: CA366242086

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522271C>T (hg19) ; chr6:g.157201137C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201137C>T , CM000668.2:g.157201137C>T	GRCh38
NC_000006.11:g.157522271C>T , CM000668.1:g.157522271C>T	GRCh37
NC_000006.10:g.157563963C>T	NCBI36
NG_032093.1:g.428208C>T
NG_032093.2:g.428208C>T
NG_066624.1:g.430112C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4753C>T	ENSP00000055163.8:p.His1585Tyr
ENST00000414678.8:c.4822C>T	ENSP00000412835.3:p.His1608Tyr
ENST00000637015.2:c.5041C>T	ENSP00000489729.2:p.His1681Tyr
ENST00000346085.10:c.4792C>T	ENSP00000344546.5:p.His1598Tyr
ENST00000350026.10:c.4504C>T	ENSP00000055163.7:p.His1502Tyr
ENST00000414678.7:c.3070C>T	ENSP00000412835.2:p.His1024Tyr
ENST00000635849.1:c.2233C>T	ENSP00000490948.1:p.His745Tyr
ENST00000635957.1:c.1864C>T	ENSP00000490385.1:p.His622Tyr
ENST00000636227.1:n.3375C>T
ENST00000636254.1:n.832C>T
ENST00000636930.2:c.4912C>T MANE Select	ENSP00000490491.2:p.His1638Tyr
ENST00000636940.1:n.2909C>T
ENST00000637015.1:c.2280C>T
ENST00000637568.1:c.2194C>T
ENST00000637741.1:n.1578C>T
ENST00000637810.1:c.2254C>T	ENSP00000489636.1:p.His752Tyr
ENST00000637904.1:c.2413C>T	ENSP00000490550.1:p.His805Tyr
ENST00000647938.1:c.4543C>T	ENSP00000498155.1:p.His1515Tyr
ENST00000346085.9:c.4543C>T	ENSP00000344546.4:p.His1515Tyr
ENST00000350026.9:c.4504C>T	ENSP00000055163.7:p.His1502Tyr
ENST00000414678.6:c.3070C>T	ENSP00000412835.2:p.His1024Tyr
NM_017519.2:c.4504C>T	NP_059989.2:p.His1502Tyr
NM_020732.3:c.4543C>T	NP_065783.3:p.His1515Tyr
XM_005267069.3:c.4663C>T	XP_005267126.2:p.His1555Tyr
XM_011535984.1:c.3742C>T	XP_011534286.1:p.His1248Tyr
XM_011535985.1:c.3562C>T	XP_011534287.1:p.His1188Tyr
XM_011535986.1:c.3322C>T	XP_011534288.1:p.His1108Tyr
XM_011535987.1:c.2941C>T	XP_011534289.1:p.His981Tyr
XM_011535988.1:c.1804C>T	XP_011534290.1:p.His602Tyr
NM_001346813.1:c.4663C>T	NP_001333742.1:p.His1555Tyr
NM_001363725.1:c.2413C>T	NP_001350654.1:p.His805Tyr
XM_011535984.2:c.4873C>T	XP_011534286.2:p.His1625Tyr
XM_011535988.3:c.1804C>T	XP_011534290.1:p.His602Tyr
XM_017011103.2:c.4774C>T	XP_016866592.1:p.His1592Tyr
XM_017011104.1:c.4744C>T	XP_016866593.1:p.His1582Tyr
XM_017011105.2:c.4714C>T	XP_016866594.1:p.His1572Tyr
XM_017011106.2:c.4585C>T	XP_016866595.1:p.His1529Tyr
XM_017011107.2:c.4564C>T	XP_016866596.1:p.His1522Tyr
XR_002956289.1:n.4859C>T
NM_001363725.2:c.2413C>T	NP_001350654.1:p.His805Tyr
NM_001371656.1:c.4792C>T	NP_001358585.1:p.His1598Tyr
NM_001374820.1:c.4792C>T	NP_001361749.1:p.His1598Tyr
NM_001374828.1:c.4912C>T MANE Select	NP_001361757.1:p.His1638Tyr
NM_017519.3:c.4753C>T	NP_059989.3:p.His1585Tyr