Canonical Allele Identifier: CA452978382

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522171T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201037T>A , CM000668.2:g.157201037T>A	GRCh38
NC_000006.11:g.157522171T>A , CM000668.1:g.157522171T>A	GRCh37
NC_000006.10:g.157563863T>A	NCBI36
NG_032093.1:g.428108T>A
NG_032093.2:g.428108T>A
NG_066624.1:g.430012T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4653T>A	ENSP00000055163.8:p.Pro1551=
ENST00000414678.8:c.4722T>A	ENSP00000412835.3:p.Pro1574=
ENST00000637015.2:c.4941T>A	ENSP00000489729.2:p.Pro1647=
ENST00000346085.10:c.4692T>A	ENSP00000344546.5:p.Pro1564=
ENST00000350026.10:c.4404T>A	ENSP00000055163.7:p.Pro1468=
ENST00000414678.7:c.2970T>A	ENSP00000412835.2:p.Pro990=
ENST00000635849.1:c.2133T>A	ENSP00000490948.1:p.Pro711=
ENST00000635957.1:c.1764T>A	ENSP00000490385.1:p.Pro588=
ENST00000636227.1:n.3275T>A
ENST00000636254.1:n.732T>A
ENST00000636930.2:c.4812T>A MANE Select	ENSP00000490491.2:p.Pro1604=
ENST00000636940.1:n.2809T>A
ENST00000637015.1:c.2180T>A
ENST00000637568.1:c.2094T>A
ENST00000637741.1:n.1478T>A
ENST00000637810.1:c.2154T>A	ENSP00000489636.1:p.Pro718=
ENST00000637904.1:c.2313T>A	ENSP00000490550.1:p.Pro771=
ENST00000647938.1:c.4443T>A	ENSP00000498155.1:p.Pro1481=
ENST00000346085.9:c.4443T>A	ENSP00000344546.4:p.Pro1481=
ENST00000350026.9:c.4404T>A	ENSP00000055163.7:p.Pro1468=
ENST00000414678.6:c.2970T>A	ENSP00000412835.2:p.Pro990=
NM_017519.2:c.4404T>A	NP_059989.2:p.Pro1468=
NM_020732.3:c.4443T>A	NP_065783.3:p.Pro1481=
XM_005267069.3:c.4563T>A	XP_005267126.2:p.Pro1521=
XM_011535984.1:c.3642T>A	XP_011534286.1:p.Pro1214=
XM_011535985.1:c.3462T>A	XP_011534287.1:p.Pro1154=
XM_011535986.1:c.3222T>A	XP_011534288.1:p.Pro1074=
XM_011535987.1:c.2841T>A	XP_011534289.1:p.Pro947=
XM_011535988.1:c.1704T>A	XP_011534290.1:p.Pro568=
NM_001346813.1:c.4563T>A	NP_001333742.1:p.Pro1521=
NM_001363725.1:c.2313T>A	NP_001350654.1:p.Pro771=
XM_011535984.2:c.4773T>A	XP_011534286.2:p.Pro1591=
XM_011535988.3:c.1704T>A	XP_011534290.1:p.Pro568=
XM_017011103.2:c.4674T>A	XP_016866592.1:p.Pro1558=
XM_017011104.1:c.4644T>A	XP_016866593.1:p.Pro1548=
XM_017011105.2:c.4614T>A	XP_016866594.1:p.Pro1538=
XM_017011106.2:c.4485T>A	XP_016866595.1:p.Pro1495=
XM_017011107.2:c.4464T>A	XP_016866596.1:p.Pro1488=
XR_002956289.1:n.4759T>A
NM_001363725.2:c.2313T>A	NP_001350654.1:p.Pro771=
NM_001371656.1:c.4692T>A	NP_001358585.1:p.Pro1564=
NM_001374820.1:c.4692T>A	NP_001361749.1:p.Pro1564=
NM_001374828.1:c.4812T>A MANE Select	NP_001361757.1:p.Pro1604=
NM_017519.3:c.4653T>A	NP_059989.3:p.Pro1551=