Canonical Allele Identifier: CA452781564

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510882T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189748T>G , CM000668.2:g.157189748T>G	GRCh38
NC_000006.11:g.157510882T>G , CM000668.1:g.157510882T>G	GRCh37
NC_000006.10:g.157552574T>G	NCBI36
NG_032093.1:g.416819T>G
NG_032093.2:g.416819T>G
NG_066624.1:g.418723T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3867T>G	ENSP00000055163.8:p.Pro1289=
ENST00000414678.8:c.3936T>G	ENSP00000412835.3:p.Pro1312=
ENST00000637015.2:c.4155T>G	ENSP00000489729.2:p.Pro1385=
ENST00000346085.10:c.3906T>G	ENSP00000344546.5:p.Pro1302=
ENST00000350026.10:c.3618T>G	ENSP00000055163.7:p.Pro1206=
ENST00000414678.7:c.2184T>G	ENSP00000412835.2:p.Pro728=
ENST00000635849.1:c.1347T>G	ENSP00000490948.1:p.Pro449=
ENST00000635957.1:c.981T>G	ENSP00000490385.1:p.Pro327=
ENST00000636930.2:c.4026T>G MANE Select	ENSP00000490491.2:p.Pro1342=
ENST00000636940.1:n.2023T>G
ENST00000637015.1:c.1394T>G
ENST00000637568.1:c.1308T>G
ENST00000637741.1:n.692T>G
ENST00000637810.1:c.1368T>G	ENSP00000489636.1:p.Pro456=
ENST00000637904.1:c.1527T>G	ENSP00000490550.1:p.Pro509=
ENST00000647938.1:c.3657T>G	ENSP00000498155.1:p.Pro1219=
ENST00000346085.9:c.3657T>G	ENSP00000344546.4:p.Pro1219=
ENST00000350026.9:c.3618T>G	ENSP00000055163.7:p.Pro1206=
ENST00000414678.6:c.2184T>G	ENSP00000412835.2:p.Pro728=
NM_017519.2:c.3618T>G	NP_059989.2:p.Pro1206=
NM_020732.3:c.3657T>G	NP_065783.3:p.Pro1219=
XM_005267069.3:c.3777T>G	XP_005267126.2:p.Pro1259=
XM_011535984.1:c.2856T>G	XP_011534286.1:p.Pro952=
XM_011535985.1:c.2676T>G	XP_011534287.1:p.Pro892=
XM_011535986.1:c.2436T>G	XP_011534288.1:p.Pro812=
XM_011535987.1:c.2055T>G	XP_011534289.1:p.Pro685=
XM_011535988.1:c.918T>G	XP_011534290.1:p.Pro306=
NM_001346813.1:c.3777T>G	NP_001333742.1:p.Pro1259=
NM_001363725.1:c.1527T>G	NP_001350654.1:p.Pro509=
XM_011535984.2:c.3987T>G	XP_011534286.2:p.Pro1329=
XM_011535988.3:c.918T>G	XP_011534290.1:p.Pro306=
XM_017011103.2:c.3888T>G	XP_016866592.1:p.Pro1296=
XM_017011104.1:c.3858T>G	XP_016866593.1:p.Pro1286=
XM_017011105.2:c.3828T>G	XP_016866594.1:p.Pro1276=
XM_017011106.2:c.3699T>G	XP_016866595.1:p.Pro1233=
XM_017011107.2:c.3678T>G	XP_016866596.1:p.Pro1226=
XR_002956289.1:n.4070T>G
NM_001363725.2:c.1527T>G	NP_001350654.1:p.Pro509=
NM_001371656.1:c.3906T>G	NP_001358585.1:p.Pro1302=
NM_001374820.1:c.3906T>G	NP_001361749.1:p.Pro1302=
NM_001374828.1:c.4026T>G MANE Select	NP_001361757.1:p.Pro1342=
NM_017519.3:c.3867T>G	NP_059989.3:p.Pro1289=