Canonical Allele Identifier: CA366242407

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522420G>T (hg19) ; chr6:g.157201286G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201286G>T , CM000668.2:g.157201286G>T	GRCh38
NC_000006.11:g.157522420G>T , CM000668.1:g.157522420G>T	GRCh37
NC_000006.10:g.157564112G>T	NCBI36
NG_032093.1:g.428357G>T
NG_032093.2:g.428357G>T
NG_066624.1:g.430261G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4902G>T	ENSP00000055163.8:p.Glu1634Asp
ENST00000414678.8:c.4971G>T	ENSP00000412835.3:p.Glu1657Asp
ENST00000637015.2:c.5190G>T	ENSP00000489729.2:p.Glu1730Asp
ENST00000346085.10:c.4941G>T	ENSP00000344546.5:p.Glu1647Asp
ENST00000350026.10:c.4653G>T	ENSP00000055163.7:p.Glu1551Asp
ENST00000414678.7:c.3219G>T	ENSP00000412835.2:p.Glu1073Asp
ENST00000635849.1:c.2382G>T	ENSP00000490948.1:p.Glu794Asp
ENST00000635957.1:c.2013G>T	ENSP00000490385.1:p.Glu671Asp
ENST00000636227.1:n.3524G>T
ENST00000636254.1:n.981G>T
ENST00000636930.2:c.5061G>T MANE Select	ENSP00000490491.2:p.Glu1687Asp
ENST00000636940.1:n.3058G>T
ENST00000637015.1:c.2429G>T
ENST00000637568.1:c.2343G>T
ENST00000637741.1:n.1727G>T
ENST00000637810.1:c.2403G>T	ENSP00000489636.1:p.Glu801Asp
ENST00000637904.1:c.2562G>T	ENSP00000490550.1:p.Glu854Asp
ENST00000647938.1:c.4692G>T	ENSP00000498155.1:p.Glu1564Asp
ENST00000346085.9:c.4692G>T	ENSP00000344546.4:p.Glu1564Asp
ENST00000350026.9:c.4653G>T	ENSP00000055163.7:p.Glu1551Asp
ENST00000414678.6:c.3219G>T	ENSP00000412835.2:p.Glu1073Asp
NM_017519.2:c.4653G>T	NP_059989.2:p.Glu1551Asp
NM_020732.3:c.4692G>T	NP_065783.3:p.Glu1564Asp
XM_005267069.3:c.4812G>T	XP_005267126.2:p.Glu1604Asp
XM_011535984.1:c.3891G>T	XP_011534286.1:p.Glu1297Asp
XM_011535985.1:c.3711G>T	XP_011534287.1:p.Glu1237Asp
XM_011535986.1:c.3471G>T	XP_011534288.1:p.Glu1157Asp
XM_011535987.1:c.3090G>T	XP_011534289.1:p.Glu1030Asp
XM_011535988.1:c.1953G>T	XP_011534290.1:p.Glu651Asp
NM_001346813.1:c.4812G>T	NP_001333742.1:p.Glu1604Asp
NM_001363725.1:c.2562G>T	NP_001350654.1:p.Glu854Asp
XM_011535984.2:c.5022G>T	XP_011534286.2:p.Glu1674Asp
XM_011535988.3:c.1953G>T	XP_011534290.1:p.Glu651Asp
XM_017011103.2:c.4923G>T	XP_016866592.1:p.Glu1641Asp
XM_017011104.1:c.4893G>T	XP_016866593.1:p.Glu1631Asp
XM_017011105.2:c.4863G>T	XP_016866594.1:p.Glu1621Asp
XM_017011106.2:c.4734G>T	XP_016866595.1:p.Glu1578Asp
XM_017011107.2:c.4713G>T	XP_016866596.1:p.Glu1571Asp
XR_002956289.1:n.5008G>T
NM_001363725.2:c.2562G>T	NP_001350654.1:p.Glu854Asp
NM_001371656.1:c.4941G>T	NP_001358585.1:p.Glu1647Asp
NM_001374820.1:c.4941G>T	NP_001361749.1:p.Glu1647Asp
NM_001374828.1:c.5061G>T MANE Select	NP_001361757.1:p.Glu1687Asp
NM_017519.3:c.4902G>T	NP_059989.3:p.Glu1634Asp