Canonical Allele Identifier: CA366242418

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522425G>T (hg19) ; chr6:g.157201291G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201291G>T , CM000668.2:g.157201291G>T	GRCh38
NC_000006.11:g.157522425G>T , CM000668.1:g.157522425G>T	GRCh37
NC_000006.10:g.157564117G>T	NCBI36
NG_032093.1:g.428362G>T
NG_032093.2:g.428362G>T
NG_066624.1:g.430266G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4907G>T	ENSP00000055163.8:p.Arg1636Leu
ENST00000414678.8:c.4976G>T	ENSP00000412835.3:p.Arg1659Leu
ENST00000637015.2:c.5195G>T	ENSP00000489729.2:p.Arg1732Leu
ENST00000346085.10:c.4946G>T	ENSP00000344546.5:p.Arg1649Leu
ENST00000350026.10:c.4658G>T	ENSP00000055163.7:p.Arg1553Leu
ENST00000414678.7:c.3224G>T	ENSP00000412835.2:p.Arg1075Leu
ENST00000635849.1:c.2387G>T	ENSP00000490948.1:p.Arg796Leu
ENST00000635957.1:c.2018G>T	ENSP00000490385.1:p.Arg673Leu
ENST00000636227.1:n.3529G>T
ENST00000636254.1:n.986G>T
ENST00000636930.2:c.5066G>T MANE Select	ENSP00000490491.2:p.Arg1689Leu
ENST00000636940.1:n.3063G>T
ENST00000637015.1:c.2434G>T
ENST00000637568.1:c.2348G>T
ENST00000637741.1:n.1732G>T
ENST00000637810.1:c.2408G>T	ENSP00000489636.1:p.Arg803Leu
ENST00000637904.1:c.2567G>T	ENSP00000490550.1:p.Arg856Leu
ENST00000647938.1:c.4697G>T	ENSP00000498155.1:p.Arg1566Leu
ENST00000346085.9:c.4697G>T	ENSP00000344546.4:p.Arg1566Leu
ENST00000350026.9:c.4658G>T	ENSP00000055163.7:p.Arg1553Leu
ENST00000414678.6:c.3224G>T	ENSP00000412835.2:p.Arg1075Leu
NM_017519.2:c.4658G>T	NP_059989.2:p.Arg1553Leu
NM_020732.3:c.4697G>T	NP_065783.3:p.Arg1566Leu
XM_005267069.3:c.4817G>T	XP_005267126.2:p.Arg1606Leu
XM_011535984.1:c.3896G>T	XP_011534286.1:p.Arg1299Leu
XM_011535985.1:c.3716G>T	XP_011534287.1:p.Arg1239Leu
XM_011535986.1:c.3476G>T	XP_011534288.1:p.Arg1159Leu
XM_011535987.1:c.3095G>T	XP_011534289.1:p.Arg1032Leu
XM_011535988.1:c.1958G>T	XP_011534290.1:p.Arg653Leu
NM_001346813.1:c.4817G>T	NP_001333742.1:p.Arg1606Leu
NM_001363725.1:c.2567G>T	NP_001350654.1:p.Arg856Leu
XM_011535984.2:c.5027G>T	XP_011534286.2:p.Arg1676Leu
XM_011535988.3:c.1958G>T	XP_011534290.1:p.Arg653Leu
XM_017011103.2:c.4928G>T	XP_016866592.1:p.Arg1643Leu
XM_017011104.1:c.4898G>T	XP_016866593.1:p.Arg1633Leu
XM_017011105.2:c.4868G>T	XP_016866594.1:p.Arg1623Leu
XM_017011106.2:c.4739G>T	XP_016866595.1:p.Arg1580Leu
XM_017011107.2:c.4718G>T	XP_016866596.1:p.Arg1573Leu
XR_002956289.1:n.5013G>T
NM_001363725.2:c.2567G>T	NP_001350654.1:p.Arg856Leu
NM_001371656.1:c.4946G>T	NP_001358585.1:p.Arg1649Leu
NM_001374820.1:c.4946G>T	NP_001361749.1:p.Arg1649Leu
NM_001374828.1:c.5066G>T MANE Select	NP_001361757.1:p.Arg1689Leu
NM_017519.3:c.4907G>T	NP_059989.3:p.Arg1636Leu