Canonical Allele Identifier: CA366241627

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522169C>A (hg19) ; chr6:g.157201035C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201035C>A , CM000668.2:g.157201035C>A	GRCh38
NC_000006.11:g.157522169C>A , CM000668.1:g.157522169C>A	GRCh37
NC_000006.10:g.157563861C>A	NCBI36
NG_032093.1:g.428106C>A
NG_032093.2:g.428106C>A
NG_066624.1:g.430010C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4651C>A	ENSP00000055163.8:p.Pro1551Thr
ENST00000414678.8:c.4720C>A	ENSP00000412835.3:p.Pro1574Thr
ENST00000637015.2:c.4939C>A	ENSP00000489729.2:p.Pro1647Thr
ENST00000346085.10:c.4690C>A	ENSP00000344546.5:p.Pro1564Thr
ENST00000350026.10:c.4402C>A	ENSP00000055163.7:p.Pro1468Thr
ENST00000414678.7:c.2968C>A	ENSP00000412835.2:p.Pro990Thr
ENST00000635849.1:c.2131C>A	ENSP00000490948.1:p.Pro711Thr
ENST00000635957.1:c.1762C>A	ENSP00000490385.1:p.Pro588Thr
ENST00000636227.1:n.3273C>A
ENST00000636254.1:n.730C>A
ENST00000636930.2:c.4810C>A MANE Select	ENSP00000490491.2:p.Pro1604Thr
ENST00000636940.1:n.2807C>A
ENST00000637015.1:c.2178C>A
ENST00000637568.1:c.2092C>A
ENST00000637741.1:n.1476C>A
ENST00000637810.1:c.2152C>A	ENSP00000489636.1:p.Pro718Thr
ENST00000637904.1:c.2311C>A	ENSP00000490550.1:p.Pro771Thr
ENST00000647938.1:c.4441C>A	ENSP00000498155.1:p.Pro1481Thr
ENST00000346085.9:c.4441C>A	ENSP00000344546.4:p.Pro1481Thr
ENST00000350026.9:c.4402C>A	ENSP00000055163.7:p.Pro1468Thr
ENST00000414678.6:c.2968C>A	ENSP00000412835.2:p.Pro990Thr
NM_017519.2:c.4402C>A	NP_059989.2:p.Pro1468Thr
NM_020732.3:c.4441C>A	NP_065783.3:p.Pro1481Thr
XM_005267069.3:c.4561C>A	XP_005267126.2:p.Pro1521Thr
XM_011535984.1:c.3640C>A	XP_011534286.1:p.Pro1214Thr
XM_011535985.1:c.3460C>A	XP_011534287.1:p.Pro1154Thr
XM_011535986.1:c.3220C>A	XP_011534288.1:p.Pro1074Thr
XM_011535987.1:c.2839C>A	XP_011534289.1:p.Pro947Thr
XM_011535988.1:c.1702C>A	XP_011534290.1:p.Pro568Thr
NM_001346813.1:c.4561C>A	NP_001333742.1:p.Pro1521Thr
NM_001363725.1:c.2311C>A	NP_001350654.1:p.Pro771Thr
XM_011535984.2:c.4771C>A	XP_011534286.2:p.Pro1591Thr
XM_011535988.3:c.1702C>A	XP_011534290.1:p.Pro568Thr
XM_017011103.2:c.4672C>A	XP_016866592.1:p.Pro1558Thr
XM_017011104.1:c.4642C>A	XP_016866593.1:p.Pro1548Thr
XM_017011105.2:c.4612C>A	XP_016866594.1:p.Pro1538Thr
XM_017011106.2:c.4483C>A	XP_016866595.1:p.Pro1495Thr
XM_017011107.2:c.4462C>A	XP_016866596.1:p.Pro1488Thr
XR_002956289.1:n.4757C>A
NM_001363725.2:c.2311C>A	NP_001350654.1:p.Pro771Thr
NM_001371656.1:c.4690C>A	NP_001358585.1:p.Pro1564Thr
NM_001374820.1:c.4690C>A	NP_001361749.1:p.Pro1564Thr
NM_001374828.1:c.4810C>A MANE Select	NP_001361757.1:p.Pro1604Thr
NM_017519.3:c.4651C>A	NP_059989.3:p.Pro1551Thr