Canonical Allele Identifier: CA366242477

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522446C>G (hg19) ; chr6:g.157201312C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201312C>G , CM000668.2:g.157201312C>G	GRCh38
NC_000006.11:g.157522446C>G , CM000668.1:g.157522446C>G	GRCh37
NC_000006.10:g.157564138C>G	NCBI36
NG_032093.1:g.428383C>G
NG_032093.2:g.428383C>G
NG_066624.1:g.430287C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4928C>G	ENSP00000055163.8:p.Pro1643Arg
ENST00000414678.8:c.4997C>G	ENSP00000412835.3:p.Pro1666Arg
ENST00000637015.2:c.5216C>G	ENSP00000489729.2:p.Pro1739Arg
ENST00000346085.10:c.4967C>G	ENSP00000344546.5:p.Pro1656Arg
ENST00000350026.10:c.4679C>G	ENSP00000055163.7:p.Pro1560Arg
ENST00000414678.7:c.3245C>G	ENSP00000412835.2:p.Pro1082Arg
ENST00000635849.1:c.2408C>G	ENSP00000490948.1:p.Pro803Arg
ENST00000635957.1:c.2039C>G	ENSP00000490385.1:p.Pro680Arg
ENST00000636227.1:n.3550C>G
ENST00000636254.1:n.1007C>G
ENST00000636930.2:c.5087C>G MANE Select	ENSP00000490491.2:p.Pro1696Arg
ENST00000636940.1:n.3084C>G
ENST00000637015.1:c.2455C>G
ENST00000637568.1:c.2369C>G
ENST00000637741.1:n.1753C>G
ENST00000637810.1:c.2429C>G	ENSP00000489636.1:p.Pro810Arg
ENST00000637904.1:c.2588C>G	ENSP00000490550.1:p.Pro863Arg
ENST00000647938.1:c.4718C>G	ENSP00000498155.1:p.Pro1573Arg
ENST00000346085.9:c.4718C>G	ENSP00000344546.4:p.Pro1573Arg
ENST00000350026.9:c.4679C>G	ENSP00000055163.7:p.Pro1560Arg
ENST00000414678.6:c.3245C>G	ENSP00000412835.2:p.Pro1082Arg
NM_017519.2:c.4679C>G	NP_059989.2:p.Pro1560Arg
NM_020732.3:c.4718C>G	NP_065783.3:p.Pro1573Arg
XM_005267069.3:c.4838C>G	XP_005267126.2:p.Pro1613Arg
XM_011535984.1:c.3917C>G	XP_011534286.1:p.Pro1306Arg
XM_011535985.1:c.3737C>G	XP_011534287.1:p.Pro1246Arg
XM_011535986.1:c.3497C>G	XP_011534288.1:p.Pro1166Arg
XM_011535987.1:c.3116C>G	XP_011534289.1:p.Pro1039Arg
XM_011535988.1:c.1979C>G	XP_011534290.1:p.Pro660Arg
NM_001346813.1:c.4838C>G	NP_001333742.1:p.Pro1613Arg
NM_001363725.1:c.2588C>G	NP_001350654.1:p.Pro863Arg
XM_011535984.2:c.5048C>G	XP_011534286.2:p.Pro1683Arg
XM_011535988.3:c.1979C>G	XP_011534290.1:p.Pro660Arg
XM_017011103.2:c.4949C>G	XP_016866592.1:p.Pro1650Arg
XM_017011104.1:c.4919C>G	XP_016866593.1:p.Pro1640Arg
XM_017011105.2:c.4889C>G	XP_016866594.1:p.Pro1630Arg
XM_017011106.2:c.4760C>G	XP_016866595.1:p.Pro1587Arg
XM_017011107.2:c.4739C>G	XP_016866596.1:p.Pro1580Arg
XR_002956289.1:n.5034C>G
NM_001363725.2:c.2588C>G	NP_001350654.1:p.Pro863Arg
NM_001371656.1:c.4967C>G	NP_001358585.1:p.Pro1656Arg
NM_001374820.1:c.4967C>G	NP_001361749.1:p.Pro1656Arg
NM_001374828.1:c.5087C>G MANE Select	NP_001361757.1:p.Pro1696Arg
NM_017519.3:c.4928C>G	NP_059989.3:p.Pro1643Arg