Canonical Allele Identifier: CA452781543

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510861A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189727A>G , CM000668.2:g.157189727A>G	GRCh38
NC_000006.11:g.157510861A>G , CM000668.1:g.157510861A>G	GRCh37
NC_000006.10:g.157552553A>G	NCBI36
NG_032093.1:g.416798A>G
NG_032093.2:g.416798A>G
NG_066624.1:g.418702A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3846A>G	ENSP00000055163.8:p.Pro1282=
ENST00000414678.8:c.3915A>G	ENSP00000412835.3:p.Pro1305=
ENST00000637015.2:c.4134A>G	ENSP00000489729.2:p.Pro1378=
ENST00000346085.10:c.3885A>G	ENSP00000344546.5:p.Pro1295=
ENST00000350026.10:c.3597A>G	ENSP00000055163.7:p.Pro1199=
ENST00000414678.7:c.2163A>G	ENSP00000412835.2:p.Pro721=
ENST00000635849.1:c.1326A>G	ENSP00000490948.1:p.Pro442=
ENST00000635957.1:c.960A>G	ENSP00000490385.1:p.Pro320=
ENST00000636930.2:c.4005A>G MANE Select	ENSP00000490491.2:p.Pro1335=
ENST00000636940.1:n.2002A>G
ENST00000637015.1:c.1373A>G
ENST00000637568.1:c.1287A>G
ENST00000637741.1:n.671A>G
ENST00000637810.1:c.1347A>G	ENSP00000489636.1:p.Pro449=
ENST00000637904.1:c.1506A>G	ENSP00000490550.1:p.Pro502=
ENST00000647938.1:c.3636A>G	ENSP00000498155.1:p.Pro1212=
ENST00000346085.9:c.3636A>G	ENSP00000344546.4:p.Pro1212=
ENST00000350026.9:c.3597A>G	ENSP00000055163.7:p.Pro1199=
ENST00000414678.6:c.2163A>G	ENSP00000412835.2:p.Pro721=
NM_017519.2:c.3597A>G	NP_059989.2:p.Pro1199=
NM_020732.3:c.3636A>G	NP_065783.3:p.Pro1212=
XM_005267069.3:c.3756A>G	XP_005267126.2:p.Pro1252=
XM_011535984.1:c.2835A>G	XP_011534286.1:p.Pro945=
XM_011535985.1:c.2655A>G	XP_011534287.1:p.Pro885=
XM_011535986.1:c.2415A>G	XP_011534288.1:p.Pro805=
XM_011535987.1:c.2034A>G	XP_011534289.1:p.Pro678=
XM_011535988.1:c.897A>G	XP_011534290.1:p.Pro299=
NM_001346813.1:c.3756A>G	NP_001333742.1:p.Pro1252=
NM_001363725.1:c.1506A>G	NP_001350654.1:p.Pro502=
XM_011535984.2:c.3966A>G	XP_011534286.2:p.Pro1322=
XM_011535988.3:c.897A>G	XP_011534290.1:p.Pro299=
XM_017011103.2:c.3867A>G	XP_016866592.1:p.Pro1289=
XM_017011104.1:c.3837A>G	XP_016866593.1:p.Pro1279=
XM_017011105.2:c.3807A>G	XP_016866594.1:p.Pro1269=
XM_017011106.2:c.3678A>G	XP_016866595.1:p.Pro1226=
XM_017011107.2:c.3657A>G	XP_016866596.1:p.Pro1219=
XR_002956289.1:n.4049A>G
NM_001363725.2:c.1506A>G	NP_001350654.1:p.Pro502=
NM_001371656.1:c.3885A>G	NP_001358585.1:p.Pro1295=
NM_001374820.1:c.3885A>G	NP_001361749.1:p.Pro1295=
NM_001374828.1:c.4005A>G MANE Select	NP_001361757.1:p.Pro1335=
NM_017519.3:c.3846A>G	NP_059989.3:p.Pro1282=