Canonical Allele Identifier: CA366234122

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338831
• MyVariant Identifiers: chr6:g.157510836C>G (hg19) ; chr6:g.157189702C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189702C>G , CM000668.2:g.157189702C>G	GRCh38
NC_000006.11:g.157510836C>G , CM000668.1:g.157510836C>G	GRCh37
NC_000006.10:g.157552528C>G	NCBI36
NG_032093.1:g.416773C>G
NG_032093.2:g.416773C>G
NG_066624.1:g.418677C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3821C>G	ENSP00000055163.8:p.Ala1274Gly
ENST00000414678.8:c.3890C>G	ENSP00000412835.3:p.Ala1297Gly
ENST00000637015.2:c.4109C>G	ENSP00000489729.2:p.Ala1370Gly
ENST00000346085.10:c.3860C>G	ENSP00000344546.5:p.Ala1287Gly
ENST00000350026.10:c.3572C>G	ENSP00000055163.7:p.Ala1191Gly
ENST00000414678.7:c.2138C>G	ENSP00000412835.2:p.Ala713Gly
ENST00000635849.1:c.1301C>G	ENSP00000490948.1:p.Ala434Gly
ENST00000635957.1:c.935C>G	ENSP00000490385.1:p.Ala312Gly
ENST00000636930.2:c.3980C>G MANE Select	ENSP00000490491.2:p.Ala1327Gly
ENST00000636940.1:n.1977C>G
ENST00000637015.1:c.1348C>G
ENST00000637568.1:c.1262C>G
ENST00000637741.1:n.646C>G
ENST00000637810.1:c.1322C>G	ENSP00000489636.1:p.Ala441Gly
ENST00000637904.1:c.1481C>G	ENSP00000490550.1:p.Ala494Gly
ENST00000647938.1:c.3611C>G	ENSP00000498155.1:p.Ala1204Gly
ENST00000346085.9:c.3611C>G	ENSP00000344546.4:p.Ala1204Gly
ENST00000350026.9:c.3572C>G	ENSP00000055163.7:p.Ala1191Gly
ENST00000414678.6:c.2138C>G	ENSP00000412835.2:p.Ala713Gly
NM_017519.2:c.3572C>G	NP_059989.2:p.Ala1191Gly
NM_020732.3:c.3611C>G	NP_065783.3:p.Ala1204Gly
XM_005267069.3:c.3731C>G	XP_005267126.2:p.Ala1244Gly
XM_011535984.1:c.2810C>G	XP_011534286.1:p.Ala937Gly
XM_011535985.1:c.2630C>G	XP_011534287.1:p.Ala877Gly
XM_011535986.1:c.2390C>G	XP_011534288.1:p.Ala797Gly
XM_011535987.1:c.2009C>G	XP_011534289.1:p.Ala670Gly
XM_011535988.1:c.872C>G	XP_011534290.1:p.Ala291Gly
NM_001346813.1:c.3731C>G	NP_001333742.1:p.Ala1244Gly
NM_001363725.1:c.1481C>G	NP_001350654.1:p.Ala494Gly
XM_011535984.2:c.3941C>G	XP_011534286.2:p.Ala1314Gly
XM_011535988.3:c.872C>G	XP_011534290.1:p.Ala291Gly
XM_017011103.2:c.3842C>G	XP_016866592.1:p.Ala1281Gly
XM_017011104.1:c.3812C>G	XP_016866593.1:p.Ala1271Gly
XM_017011105.2:c.3782C>G	XP_016866594.1:p.Ala1261Gly
XM_017011106.2:c.3653C>G	XP_016866595.1:p.Ala1218Gly
XM_017011107.2:c.3632C>G	XP_016866596.1:p.Ala1211Gly
XR_002956289.1:n.4024C>G
NM_001363725.2:c.1481C>G	NP_001350654.1:p.Ala494Gly
NM_001371656.1:c.3860C>G	NP_001358585.1:p.Ala1287Gly
NM_001374820.1:c.3860C>G	NP_001361749.1:p.Ala1287Gly
NM_001374828.1:c.3980C>G MANE Select	NP_001361757.1:p.Ala1327Gly
NM_017519.3:c.3821C>G	NP_059989.3:p.Ala1274Gly