Canonical Allele Identifier: CA366242090

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522273C>A (hg19) ; chr6:g.157201139C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201139C>A , CM000668.2:g.157201139C>A	GRCh38
NC_000006.11:g.157522273C>A , CM000668.1:g.157522273C>A	GRCh37
NC_000006.10:g.157563965C>A	NCBI36
NG_032093.1:g.428210C>A
NG_032093.2:g.428210C>A
NG_066624.1:g.430114C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4755C>A	ENSP00000055163.8:p.His1585Gln
ENST00000414678.8:c.4824C>A	ENSP00000412835.3:p.His1608Gln
ENST00000637015.2:c.5043C>A	ENSP00000489729.2:p.His1681Gln
ENST00000346085.10:c.4794C>A	ENSP00000344546.5:p.His1598Gln
ENST00000350026.10:c.4506C>A	ENSP00000055163.7:p.His1502Gln
ENST00000414678.7:c.3072C>A	ENSP00000412835.2:p.His1024Gln
ENST00000635849.1:c.2235C>A	ENSP00000490948.1:p.His745Gln
ENST00000635957.1:c.1866C>A	ENSP00000490385.1:p.His622Gln
ENST00000636227.1:n.3377C>A
ENST00000636254.1:n.834C>A
ENST00000636930.2:c.4914C>A MANE Select	ENSP00000490491.2:p.His1638Gln
ENST00000636940.1:n.2911C>A
ENST00000637015.1:c.2282C>A
ENST00000637568.1:c.2196C>A
ENST00000637741.1:n.1580C>A
ENST00000637810.1:c.2256C>A	ENSP00000489636.1:p.His752Gln
ENST00000637904.1:c.2415C>A	ENSP00000490550.1:p.His805Gln
ENST00000647938.1:c.4545C>A	ENSP00000498155.1:p.His1515Gln
ENST00000346085.9:c.4545C>A	ENSP00000344546.4:p.His1515Gln
ENST00000350026.9:c.4506C>A	ENSP00000055163.7:p.His1502Gln
ENST00000414678.6:c.3072C>A	ENSP00000412835.2:p.His1024Gln
NM_017519.2:c.4506C>A	NP_059989.2:p.His1502Gln
NM_020732.3:c.4545C>A	NP_065783.3:p.His1515Gln
XM_005267069.3:c.4665C>A	XP_005267126.2:p.His1555Gln
XM_011535984.1:c.3744C>A	XP_011534286.1:p.His1248Gln
XM_011535985.1:c.3564C>A	XP_011534287.1:p.His1188Gln
XM_011535986.1:c.3324C>A	XP_011534288.1:p.His1108Gln
XM_011535987.1:c.2943C>A	XP_011534289.1:p.His981Gln
XM_011535988.1:c.1806C>A	XP_011534290.1:p.His602Gln
NM_001346813.1:c.4665C>A	NP_001333742.1:p.His1555Gln
NM_001363725.1:c.2415C>A	NP_001350654.1:p.His805Gln
XM_011535984.2:c.4875C>A	XP_011534286.2:p.His1625Gln
XM_011535988.3:c.1806C>A	XP_011534290.1:p.His602Gln
XM_017011103.2:c.4776C>A	XP_016866592.1:p.His1592Gln
XM_017011104.1:c.4746C>A	XP_016866593.1:p.His1582Gln
XM_017011105.2:c.4716C>A	XP_016866594.1:p.His1572Gln
XM_017011106.2:c.4587C>A	XP_016866595.1:p.His1529Gln
XM_017011107.2:c.4566C>A	XP_016866596.1:p.His1522Gln
XR_002956289.1:n.4861C>A
NM_001363725.2:c.2415C>A	NP_001350654.1:p.His805Gln
NM_001371656.1:c.4794C>A	NP_001358585.1:p.His1598Gln
NM_001374820.1:c.4794C>A	NP_001361749.1:p.His1598Gln
NM_001374828.1:c.4914C>A MANE Select	NP_001361757.1:p.His1638Gln
NM_017519.3:c.4755C>A	NP_059989.3:p.His1585Gln