Canonical Allele Identifier: CA366234732

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511187T>A (hg19) ; chr6:g.157190053T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190053T>A , CM000668.2:g.157190053T>A	GRCh38
NC_000006.11:g.157511187T>A , CM000668.1:g.157511187T>A	GRCh37
NC_000006.10:g.157552879T>A	NCBI36
NG_032093.1:g.417124T>A
NG_032093.2:g.417124T>A
NG_066624.1:g.419028T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3915T>A	ENSP00000055163.8:p.Ser1305Arg
ENST00000414678.8:c.3984T>A	ENSP00000412835.3:p.Ser1328Arg
ENST00000637015.2:c.4203T>A	ENSP00000489729.2:p.Ser1401Arg
ENST00000346085.10:c.3954T>A	ENSP00000344546.5:p.Ser1318Arg
ENST00000350026.10:c.3666T>A	ENSP00000055163.7:p.Ser1222Arg
ENST00000414678.7:c.2232T>A	ENSP00000412835.2:p.Ser744Arg
ENST00000635849.1:c.1395T>A	ENSP00000490948.1:p.Ser465Arg
ENST00000635957.1:c.1026T>A	ENSP00000490385.1:p.Ser342Arg
ENST00000636930.2:c.4074T>A MANE Select	ENSP00000490491.2:p.Ser1358Arg
ENST00000636940.1:n.2071T>A
ENST00000637015.1:c.1442T>A
ENST00000637568.1:c.1356T>A
ENST00000637741.1:n.740T>A
ENST00000637810.1:c.1416T>A	ENSP00000489636.1:p.Ser472Arg
ENST00000637904.1:c.1575T>A	ENSP00000490550.1:p.Ser525Arg
ENST00000647938.1:c.3705T>A	ENSP00000498155.1:p.Ser1235Arg
ENST00000346085.9:c.3705T>A	ENSP00000344546.4:p.Ser1235Arg
ENST00000350026.9:c.3666T>A	ENSP00000055163.7:p.Ser1222Arg
ENST00000414678.6:c.2232T>A	ENSP00000412835.2:p.Ser744Arg
NM_017519.2:c.3666T>A	NP_059989.2:p.Ser1222Arg
NM_020732.3:c.3705T>A	NP_065783.3:p.Ser1235Arg
XM_005267069.3:c.3825T>A	XP_005267126.2:p.Ser1275Arg
XM_011535984.1:c.2904T>A	XP_011534286.1:p.Ser968Arg
XM_011535985.1:c.2724T>A	XP_011534287.1:p.Ser908Arg
XM_011535986.1:c.2484T>A	XP_011534288.1:p.Ser828Arg
XM_011535987.1:c.2103T>A	XP_011534289.1:p.Ser701Arg
XM_011535988.1:c.966T>A	XP_011534290.1:p.Ser322Arg
NM_001346813.1:c.3825T>A	NP_001333742.1:p.Ser1275Arg
NM_001363725.1:c.1575T>A	NP_001350654.1:p.Ser525Arg
XM_011535984.2:c.4035T>A	XP_011534286.2:p.Ser1345Arg
XM_011535988.3:c.966T>A	XP_011534290.1:p.Ser322Arg
XM_017011103.2:c.3936T>A	XP_016866592.1:p.Ser1312Arg
XM_017011104.1:c.3906T>A	XP_016866593.1:p.Ser1302Arg
XM_017011105.2:c.3876T>A	XP_016866594.1:p.Ser1292Arg
XM_017011106.2:c.3747T>A	XP_016866595.1:p.Ser1249Arg
XM_017011107.2:c.3726T>A	XP_016866596.1:p.Ser1242Arg
XR_002956289.1:n.4118T>A
NM_001363725.2:c.1575T>A	NP_001350654.1:p.Ser525Arg
NM_001371656.1:c.3954T>A	NP_001358585.1:p.Ser1318Arg
NM_001374820.1:c.3954T>A	NP_001361749.1:p.Ser1318Arg
NM_001374828.1:c.4074T>A MANE Select	NP_001361757.1:p.Ser1358Arg
NM_017519.3:c.3915T>A	NP_059989.3:p.Ser1305Arg