Canonical Allele Identifier: CA366234095

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510825C>G (hg19) ; chr6:g.157189691C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189691C>G , CM000668.2:g.157189691C>G	GRCh38
NC_000006.11:g.157510825C>G , CM000668.1:g.157510825C>G	GRCh37
NC_000006.10:g.157552517C>G	NCBI36
NG_032093.1:g.416762C>G
NG_032093.2:g.416762C>G
NG_066624.1:g.418666C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3810C>G	ENSP00000055163.8:p.Ser1270Arg
ENST00000414678.8:c.3879C>G	ENSP00000412835.3:p.Ser1293Arg
ENST00000637015.2:c.4098C>G	ENSP00000489729.2:p.Ser1366Arg
ENST00000346085.10:c.3849C>G	ENSP00000344546.5:p.Ser1283Arg
ENST00000350026.10:c.3561C>G	ENSP00000055163.7:p.Ser1187Arg
ENST00000414678.7:c.2127C>G	ENSP00000412835.2:p.Ser709Arg
ENST00000635849.1:c.1290C>G	ENSP00000490948.1:p.Ser430Arg
ENST00000635957.1:c.924C>G	ENSP00000490385.1:p.Ser308Arg
ENST00000636930.2:c.3969C>G MANE Select	ENSP00000490491.2:p.Ser1323Arg
ENST00000636940.1:n.1966C>G
ENST00000637015.1:c.1337C>G
ENST00000637568.1:c.1251C>G
ENST00000637741.1:n.635C>G
ENST00000637810.1:c.1311C>G	ENSP00000489636.1:p.Ser437Arg
ENST00000637904.1:c.1470C>G	ENSP00000490550.1:p.Ser490Arg
ENST00000647938.1:c.3600C>G	ENSP00000498155.1:p.Ser1200Arg
ENST00000346085.9:c.3600C>G	ENSP00000344546.4:p.Ser1200Arg
ENST00000350026.9:c.3561C>G	ENSP00000055163.7:p.Ser1187Arg
ENST00000414678.6:c.2127C>G	ENSP00000412835.2:p.Ser709Arg
NM_017519.2:c.3561C>G	NP_059989.2:p.Ser1187Arg
NM_020732.3:c.3600C>G	NP_065783.3:p.Ser1200Arg
XM_005267069.3:c.3720C>G	XP_005267126.2:p.Ser1240Arg
XM_011535984.1:c.2799C>G	XP_011534286.1:p.Ser933Arg
XM_011535985.1:c.2619C>G	XP_011534287.1:p.Ser873Arg
XM_011535986.1:c.2379C>G	XP_011534288.1:p.Ser793Arg
XM_011535987.1:c.1998C>G	XP_011534289.1:p.Ser666Arg
XM_011535988.1:c.861C>G	XP_011534290.1:p.Ser287Arg
NM_001346813.1:c.3720C>G	NP_001333742.1:p.Ser1240Arg
NM_001363725.1:c.1470C>G	NP_001350654.1:p.Ser490Arg
XM_011535984.2:c.3930C>G	XP_011534286.2:p.Ser1310Arg
XM_011535988.3:c.861C>G	XP_011534290.1:p.Ser287Arg
XM_017011103.2:c.3831C>G	XP_016866592.1:p.Ser1277Arg
XM_017011104.1:c.3801C>G	XP_016866593.1:p.Ser1267Arg
XM_017011105.2:c.3771C>G	XP_016866594.1:p.Ser1257Arg
XM_017011106.2:c.3642C>G	XP_016866595.1:p.Ser1214Arg
XM_017011107.2:c.3621C>G	XP_016866596.1:p.Ser1207Arg
XR_002956289.1:n.4013C>G
NM_001363725.2:c.1470C>G	NP_001350654.1:p.Ser490Arg
NM_001371656.1:c.3849C>G	NP_001358585.1:p.Ser1283Arg
NM_001374820.1:c.3849C>G	NP_001361749.1:p.Ser1283Arg
NM_001374828.1:c.3969C>G MANE Select	NP_001361757.1:p.Ser1323Arg
NM_017519.3:c.3810C>G	NP_059989.3:p.Ser1270Arg