Canonical Allele Identifier: CA452781604

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511220A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190086A>C , CM000668.2:g.157190086A>C	GRCh38
NC_000006.11:g.157511220A>C , CM000668.1:g.157511220A>C	GRCh37
NC_000006.10:g.157552912A>C	NCBI36
NG_032093.1:g.417157A>C
NG_032093.2:g.417157A>C
NG_066624.1:g.419061A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3948A>C	ENSP00000055163.8:p.Ser1316=
ENST00000414678.8:c.4017A>C	ENSP00000412835.3:p.Ser1339=
ENST00000637015.2:c.4236A>C	ENSP00000489729.2:p.Ser1412=
ENST00000346085.10:c.3987A>C	ENSP00000344546.5:p.Ser1329=
ENST00000350026.10:c.3699A>C	ENSP00000055163.7:p.Ser1233=
ENST00000414678.7:c.2265A>C	ENSP00000412835.2:p.Ser755=
ENST00000635849.1:c.1428A>C	ENSP00000490948.1:p.Ser476=
ENST00000635957.1:c.1059A>C	ENSP00000490385.1:p.Ser353=
ENST00000636930.2:c.4107A>C MANE Select	ENSP00000490491.2:p.Ser1369=
ENST00000636940.1:n.2104A>C
ENST00000637015.1:c.1475A>C
ENST00000637568.1:c.1389A>C
ENST00000637741.1:n.773A>C
ENST00000637810.1:c.1449A>C	ENSP00000489636.1:p.Ser483=
ENST00000637904.1:c.1608A>C	ENSP00000490550.1:p.Ser536=
ENST00000647938.1:c.3738A>C	ENSP00000498155.1:p.Ser1246=
ENST00000346085.9:c.3738A>C	ENSP00000344546.4:p.Ser1246=
ENST00000350026.9:c.3699A>C	ENSP00000055163.7:p.Ser1233=
ENST00000414678.6:c.2265A>C	ENSP00000412835.2:p.Ser755=
NM_017519.2:c.3699A>C	NP_059989.2:p.Ser1233=
NM_020732.3:c.3738A>C	NP_065783.3:p.Ser1246=
XM_005267069.3:c.3858A>C	XP_005267126.2:p.Ser1286=
XM_011535984.1:c.2937A>C	XP_011534286.1:p.Ser979=
XM_011535985.1:c.2757A>C	XP_011534287.1:p.Ser919=
XM_011535986.1:c.2517A>C	XP_011534288.1:p.Ser839=
XM_011535987.1:c.2136A>C	XP_011534289.1:p.Ser712=
XM_011535988.1:c.999A>C	XP_011534290.1:p.Ser333=
NM_001346813.1:c.3858A>C	NP_001333742.1:p.Ser1286=
NM_001363725.1:c.1608A>C	NP_001350654.1:p.Ser536=
XM_011535984.2:c.4068A>C	XP_011534286.2:p.Ser1356=
XM_011535988.3:c.999A>C	XP_011534290.1:p.Ser333=
XM_017011103.2:c.3969A>C	XP_016866592.1:p.Ser1323=
XM_017011104.1:c.3939A>C	XP_016866593.1:p.Ser1313=
XM_017011105.2:c.3909A>C	XP_016866594.1:p.Ser1303=
XM_017011106.2:c.3780A>C	XP_016866595.1:p.Ser1260=
XM_017011107.2:c.3759A>C	XP_016866596.1:p.Ser1253=
XR_002956289.1:n.4151A>C
NM_001363725.2:c.1608A>C	NP_001350654.1:p.Ser536=
NM_001371656.1:c.3987A>C	NP_001358585.1:p.Ser1329=
NM_001374820.1:c.3987A>C	NP_001361749.1:p.Ser1329=
NM_001374828.1:c.4107A>C MANE Select	NP_001361757.1:p.Ser1369=
NM_017519.3:c.3948A>C	NP_059989.3:p.Ser1316=