Canonical Allele Identifier: CA452781495

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510789C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189655C>G , CM000668.2:g.157189655C>G	GRCh38
NC_000006.11:g.157510789C>G , CM000668.1:g.157510789C>G	GRCh37
NC_000006.10:g.157552481C>G	NCBI36
NG_032093.1:g.416726C>G
NG_032093.2:g.416726C>G
NG_066624.1:g.418630C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3774C>G	ENSP00000055163.8:p.Ser1258=
ENST00000414678.8:c.3843C>G	ENSP00000412835.3:p.Ser1281=
ENST00000637015.2:c.4062C>G	ENSP00000489729.2:p.Ser1354=
ENST00000346085.10:c.3813C>G	ENSP00000344546.5:p.Ser1271=
ENST00000350026.10:c.3525C>G	ENSP00000055163.7:p.Ser1175=
ENST00000414678.7:c.2091C>G	ENSP00000412835.2:p.Ser697=
ENST00000635849.1:c.1254C>G	ENSP00000490948.1:p.Ser418=
ENST00000635957.1:c.888C>G	ENSP00000490385.1:p.Ser296=
ENST00000636930.2:c.3933C>G MANE Select	ENSP00000490491.2:p.Ser1311=
ENST00000636940.1:n.1930C>G
ENST00000637015.1:c.1301C>G
ENST00000637568.1:c.1215C>G
ENST00000637741.1:n.599C>G
ENST00000637810.1:c.1275C>G	ENSP00000489636.1:p.Ser425=
ENST00000637904.1:c.1434C>G	ENSP00000490550.1:p.Ser478=
ENST00000647938.1:c.3564C>G	ENSP00000498155.1:p.Ser1188=
ENST00000346085.9:c.3564C>G	ENSP00000344546.4:p.Ser1188=
ENST00000350026.9:c.3525C>G	ENSP00000055163.7:p.Ser1175=
ENST00000414678.6:c.2091C>G	ENSP00000412835.2:p.Ser697=
NM_017519.2:c.3525C>G	NP_059989.2:p.Ser1175=
NM_020732.3:c.3564C>G	NP_065783.3:p.Ser1188=
XM_005267069.3:c.3684C>G	XP_005267126.2:p.Ser1228=
XM_011535984.1:c.2763C>G	XP_011534286.1:p.Ser921=
XM_011535985.1:c.2583C>G	XP_011534287.1:p.Ser861=
XM_011535986.1:c.2343C>G	XP_011534288.1:p.Ser781=
XM_011535987.1:c.1962C>G	XP_011534289.1:p.Ser654=
XM_011535988.1:c.825C>G	XP_011534290.1:p.Ser275=
NM_001346813.1:c.3684C>G	NP_001333742.1:p.Ser1228=
NM_001363725.1:c.1434C>G	NP_001350654.1:p.Ser478=
XM_011535984.2:c.3894C>G	XP_011534286.2:p.Ser1298=
XM_011535988.3:c.825C>G	XP_011534290.1:p.Ser275=
XM_017011103.2:c.3795C>G	XP_016866592.1:p.Ser1265=
XM_017011104.1:c.3765C>G	XP_016866593.1:p.Ser1255=
XM_017011105.2:c.3735C>G	XP_016866594.1:p.Ser1245=
XM_017011106.2:c.3606C>G	XP_016866595.1:p.Ser1202=
XM_017011107.2:c.3585C>G	XP_016866596.1:p.Ser1195=
XR_002956289.1:n.3977C>G
NM_001363725.2:c.1434C>G	NP_001350654.1:p.Ser478=
NM_001371656.1:c.3813C>G	NP_001358585.1:p.Ser1271=
NM_001374820.1:c.3813C>G	NP_001361749.1:p.Ser1271=
NM_001374828.1:c.3933C>G MANE Select	NP_001361757.1:p.Ser1311=
NM_017519.3:c.3774C>G	NP_059989.3:p.Ser1258=