Canonical Allele Identifier: CA366241649

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522172G>T (hg19) ; chr6:g.157201038G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201038G>T , CM000668.2:g.157201038G>T	GRCh38
NC_000006.11:g.157522172G>T , CM000668.1:g.157522172G>T	GRCh37
NC_000006.10:g.157563864G>T	NCBI36
NG_032093.1:g.428109G>T
NG_032093.2:g.428109G>T
NG_066624.1:g.430013G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4654G>T	ENSP00000055163.8:p.Gly1552Cys
ENST00000414678.8:c.4723G>T	ENSP00000412835.3:p.Gly1575Cys
ENST00000637015.2:c.4942G>T	ENSP00000489729.2:p.Gly1648Cys
ENST00000346085.10:c.4693G>T	ENSP00000344546.5:p.Gly1565Cys
ENST00000350026.10:c.4405G>T	ENSP00000055163.7:p.Gly1469Cys
ENST00000414678.7:c.2971G>T	ENSP00000412835.2:p.Gly991Cys
ENST00000635849.1:c.2134G>T	ENSP00000490948.1:p.Gly712Cys
ENST00000635957.1:c.1765G>T	ENSP00000490385.1:p.Gly589Cys
ENST00000636227.1:n.3276G>T
ENST00000636254.1:n.733G>T
ENST00000636930.2:c.4813G>T MANE Select	ENSP00000490491.2:p.Gly1605Cys
ENST00000636940.1:n.2810G>T
ENST00000637015.1:c.2181G>T
ENST00000637568.1:c.2095G>T
ENST00000637741.1:n.1479G>T
ENST00000637810.1:c.2155G>T	ENSP00000489636.1:p.Gly719Cys
ENST00000637904.1:c.2314G>T	ENSP00000490550.1:p.Gly772Cys
ENST00000647938.1:c.4444G>T	ENSP00000498155.1:p.Gly1482Cys
ENST00000346085.9:c.4444G>T	ENSP00000344546.4:p.Gly1482Cys
ENST00000350026.9:c.4405G>T	ENSP00000055163.7:p.Gly1469Cys
ENST00000414678.6:c.2971G>T	ENSP00000412835.2:p.Gly991Cys
NM_017519.2:c.4405G>T	NP_059989.2:p.Gly1469Cys
NM_020732.3:c.4444G>T	NP_065783.3:p.Gly1482Cys
XM_005267069.3:c.4564G>T	XP_005267126.2:p.Gly1522Cys
XM_011535984.1:c.3643G>T	XP_011534286.1:p.Gly1215Cys
XM_011535985.1:c.3463G>T	XP_011534287.1:p.Gly1155Cys
XM_011535986.1:c.3223G>T	XP_011534288.1:p.Gly1075Cys
XM_011535987.1:c.2842G>T	XP_011534289.1:p.Gly948Cys
XM_011535988.1:c.1705G>T	XP_011534290.1:p.Gly569Cys
NM_001346813.1:c.4564G>T	NP_001333742.1:p.Gly1522Cys
NM_001363725.1:c.2314G>T	NP_001350654.1:p.Gly772Cys
XM_011535984.2:c.4774G>T	XP_011534286.2:p.Gly1592Cys
XM_011535988.3:c.1705G>T	XP_011534290.1:p.Gly569Cys
XM_017011103.2:c.4675G>T	XP_016866592.1:p.Gly1559Cys
XM_017011104.1:c.4645G>T	XP_016866593.1:p.Gly1549Cys
XM_017011105.2:c.4615G>T	XP_016866594.1:p.Gly1539Cys
XM_017011106.2:c.4486G>T	XP_016866595.1:p.Gly1496Cys
XM_017011107.2:c.4465G>T	XP_016866596.1:p.Gly1489Cys
XR_002956289.1:n.4760G>T
NM_001363725.2:c.2314G>T	NP_001350654.1:p.Gly772Cys
NM_001371656.1:c.4693G>T	NP_001358585.1:p.Gly1565Cys
NM_001374820.1:c.4693G>T	NP_001361749.1:p.Gly1565Cys
NM_001374828.1:c.4813G>T MANE Select	NP_001361757.1:p.Gly1605Cys
NM_017519.3:c.4654G>T	NP_059989.3:p.Gly1552Cys