Canonical Allele Identifier: CA366242084

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4753C>A	ENSP00000055163.8:p.His1585Asn
ENST00000414678.8:c.4822C>A	ENSP00000412835.3:p.His1608Asn
ENST00000637015.2:c.5041C>A	ENSP00000489729.2:p.His1681Asn
ENST00000346085.10:c.4792C>A	ENSP00000344546.5:p.His1598Asn
ENST00000350026.10:c.4504C>A	ENSP00000055163.7:p.His1502Asn
ENST00000414678.7:c.3070C>A	ENSP00000412835.2:p.His1024Asn
ENST00000635849.1:c.2233C>A	ENSP00000490948.1:p.His745Asn
ENST00000635957.1:c.1864C>A	ENSP00000490385.1:p.His622Asn
ENST00000636227.1:n.3375C>A
ENST00000636254.1:n.832C>A
ENST00000636930.2:c.4912C>A MANE Select	ENSP00000490491.2:p.His1638Asn
ENST00000636940.1:n.2909C>A
ENST00000637015.1:c.2280C>A
ENST00000637568.1:c.2194C>A
ENST00000637741.1:n.1578C>A
ENST00000637810.1:c.2254C>A	ENSP00000489636.1:p.His752Asn
ENST00000637904.1:c.2413C>A	ENSP00000490550.1:p.His805Asn
ENST00000647938.1:c.4543C>A	ENSP00000498155.1:p.His1515Asn
ENST00000346085.9:c.4543C>A	ENSP00000344546.4:p.His1515Asn
ENST00000350026.9:c.4504C>A	ENSP00000055163.7:p.His1502Asn
ENST00000414678.6:c.3070C>A	ENSP00000412835.2:p.His1024Asn
NM_017519.2:c.4504C>A	NP_059989.2:p.His1502Asn
NM_020732.3:c.4543C>A	NP_065783.3:p.His1515Asn
XM_005267069.3:c.4663C>A	XP_005267126.2:p.His1555Asn
XM_011535984.1:c.3742C>A	XP_011534286.1:p.His1248Asn
XM_011535985.1:c.3562C>A	XP_011534287.1:p.His1188Asn
XM_011535986.1:c.3322C>A	XP_011534288.1:p.His1108Asn
XM_011535987.1:c.2941C>A	XP_011534289.1:p.His981Asn
XM_011535988.1:c.1804C>A	XP_011534290.1:p.His602Asn
NM_001346813.1:c.4663C>A	NP_001333742.1:p.His1555Asn
NM_001363725.1:c.2413C>A	NP_001350654.1:p.His805Asn
XM_011535984.2:c.4873C>A	XP_011534286.2:p.His1625Asn
XM_011535988.3:c.1804C>A	XP_011534290.1:p.His602Asn
XM_017011103.2:c.4774C>A	XP_016866592.1:p.His1592Asn
XM_017011104.1:c.4744C>A	XP_016866593.1:p.His1582Asn
XM_017011105.2:c.4714C>A	XP_016866594.1:p.His1572Asn
XM_017011106.2:c.4585C>A	XP_016866595.1:p.His1529Asn
XM_017011107.2:c.4564C>A	XP_016866596.1:p.His1522Asn
XR_002956289.1:n.4859C>A
NM_001363725.2:c.2413C>A	NP_001350654.1:p.His805Asn
NM_001371656.1:c.4792C>A	NP_001358585.1:p.His1598Asn
NM_001374820.1:c.4792C>A	NP_001361749.1:p.His1598Asn
NM_001374828.1:c.4912C>A MANE Select	NP_001361757.1:p.His1638Asn
NM_017519.3:c.4753C>A	NP_059989.3:p.His1585Asn