Canonical Allele Identifier: CA366242088

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522272A>G (hg19) ; chr6:g.157201138A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201138A>G , CM000668.2:g.157201138A>G	GRCh38
NC_000006.11:g.157522272A>G , CM000668.1:g.157522272A>G	GRCh37
NC_000006.10:g.157563964A>G	NCBI36
NG_032093.1:g.428209A>G
NG_032093.2:g.428209A>G
NG_066624.1:g.430113A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4754A>G	ENSP00000055163.8:p.His1585Arg
ENST00000414678.8:c.4823A>G	ENSP00000412835.3:p.His1608Arg
ENST00000637015.2:c.5042A>G	ENSP00000489729.2:p.His1681Arg
ENST00000346085.10:c.4793A>G	ENSP00000344546.5:p.His1598Arg
ENST00000350026.10:c.4505A>G	ENSP00000055163.7:p.His1502Arg
ENST00000414678.7:c.3071A>G	ENSP00000412835.2:p.His1024Arg
ENST00000635849.1:c.2234A>G	ENSP00000490948.1:p.His745Arg
ENST00000635957.1:c.1865A>G	ENSP00000490385.1:p.His622Arg
ENST00000636227.1:n.3376A>G
ENST00000636254.1:n.833A>G
ENST00000636930.2:c.4913A>G MANE Select	ENSP00000490491.2:p.His1638Arg
ENST00000636940.1:n.2910A>G
ENST00000637015.1:c.2281A>G
ENST00000637568.1:c.2195A>G
ENST00000637741.1:n.1579A>G
ENST00000637810.1:c.2255A>G	ENSP00000489636.1:p.His752Arg
ENST00000637904.1:c.2414A>G	ENSP00000490550.1:p.His805Arg
ENST00000647938.1:c.4544A>G	ENSP00000498155.1:p.His1515Arg
ENST00000346085.9:c.4544A>G	ENSP00000344546.4:p.His1515Arg
ENST00000350026.9:c.4505A>G	ENSP00000055163.7:p.His1502Arg
ENST00000414678.6:c.3071A>G	ENSP00000412835.2:p.His1024Arg
NM_017519.2:c.4505A>G	NP_059989.2:p.His1502Arg
NM_020732.3:c.4544A>G	NP_065783.3:p.His1515Arg
XM_005267069.3:c.4664A>G	XP_005267126.2:p.His1555Arg
XM_011535984.1:c.3743A>G	XP_011534286.1:p.His1248Arg
XM_011535985.1:c.3563A>G	XP_011534287.1:p.His1188Arg
XM_011535986.1:c.3323A>G	XP_011534288.1:p.His1108Arg
XM_011535987.1:c.2942A>G	XP_011534289.1:p.His981Arg
XM_011535988.1:c.1805A>G	XP_011534290.1:p.His602Arg
NM_001346813.1:c.4664A>G	NP_001333742.1:p.His1555Arg
NM_001363725.1:c.2414A>G	NP_001350654.1:p.His805Arg
XM_011535984.2:c.4874A>G	XP_011534286.2:p.His1625Arg
XM_011535988.3:c.1805A>G	XP_011534290.1:p.His602Arg
XM_017011103.2:c.4775A>G	XP_016866592.1:p.His1592Arg
XM_017011104.1:c.4745A>G	XP_016866593.1:p.His1582Arg
XM_017011105.2:c.4715A>G	XP_016866594.1:p.His1572Arg
XM_017011106.2:c.4586A>G	XP_016866595.1:p.His1529Arg
XM_017011107.2:c.4565A>G	XP_016866596.1:p.His1522Arg
XR_002956289.1:n.4860A>G
NM_001363725.2:c.2414A>G	NP_001350654.1:p.His805Arg
NM_001371656.1:c.4793A>G	NP_001358585.1:p.His1598Arg
NM_001374820.1:c.4793A>G	NP_001361749.1:p.His1598Arg
NM_001374828.1:c.4913A>G MANE Select	NP_001361757.1:p.His1638Arg
NM_017519.3:c.4754A>G	NP_059989.3:p.His1585Arg