Canonical Allele Identifier: CA366234129

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510839A>T (hg19) ; chr6:g.157189705A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189705A>T , CM000668.2:g.157189705A>T	GRCh38
NC_000006.11:g.157510839A>T , CM000668.1:g.157510839A>T	GRCh37
NC_000006.10:g.157552531A>T	NCBI36
NG_032093.1:g.416776A>T
NG_032093.2:g.416776A>T
NG_066624.1:g.418680A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3824A>T	ENSP00000055163.8:p.Glu1275Val
ENST00000414678.8:c.3893A>T	ENSP00000412835.3:p.Glu1298Val
ENST00000637015.2:c.4112A>T	ENSP00000489729.2:p.Glu1371Val
ENST00000346085.10:c.3863A>T	ENSP00000344546.5:p.Glu1288Val
ENST00000350026.10:c.3575A>T	ENSP00000055163.7:p.Glu1192Val
ENST00000414678.7:c.2141A>T	ENSP00000412835.2:p.Glu714Val
ENST00000635849.1:c.1304A>T	ENSP00000490948.1:p.Glu435Val
ENST00000635957.1:c.938A>T	ENSP00000490385.1:p.Glu313Val
ENST00000636930.2:c.3983A>T MANE Select	ENSP00000490491.2:p.Glu1328Val
ENST00000636940.1:n.1980A>T
ENST00000637015.1:c.1351A>T
ENST00000637568.1:c.1265A>T
ENST00000637741.1:n.649A>T
ENST00000637810.1:c.1325A>T	ENSP00000489636.1:p.Glu442Val
ENST00000637904.1:c.1484A>T	ENSP00000490550.1:p.Glu495Val
ENST00000647938.1:c.3614A>T	ENSP00000498155.1:p.Glu1205Val
ENST00000346085.9:c.3614A>T	ENSP00000344546.4:p.Glu1205Val
ENST00000350026.9:c.3575A>T	ENSP00000055163.7:p.Glu1192Val
ENST00000414678.6:c.2141A>T	ENSP00000412835.2:p.Glu714Val
NM_017519.2:c.3575A>T	NP_059989.2:p.Glu1192Val
NM_020732.3:c.3614A>T	NP_065783.3:p.Glu1205Val
XM_005267069.3:c.3734A>T	XP_005267126.2:p.Glu1245Val
XM_011535984.1:c.2813A>T	XP_011534286.1:p.Glu938Val
XM_011535985.1:c.2633A>T	XP_011534287.1:p.Glu878Val
XM_011535986.1:c.2393A>T	XP_011534288.1:p.Glu798Val
XM_011535987.1:c.2012A>T	XP_011534289.1:p.Glu671Val
XM_011535988.1:c.875A>T	XP_011534290.1:p.Glu292Val
NM_001346813.1:c.3734A>T	NP_001333742.1:p.Glu1245Val
NM_001363725.1:c.1484A>T	NP_001350654.1:p.Glu495Val
XM_011535984.2:c.3944A>T	XP_011534286.2:p.Glu1315Val
XM_011535988.3:c.875A>T	XP_011534290.1:p.Glu292Val
XM_017011103.2:c.3845A>T	XP_016866592.1:p.Glu1282Val
XM_017011104.1:c.3815A>T	XP_016866593.1:p.Glu1272Val
XM_017011105.2:c.3785A>T	XP_016866594.1:p.Glu1262Val
XM_017011106.2:c.3656A>T	XP_016866595.1:p.Glu1219Val
XM_017011107.2:c.3635A>T	XP_016866596.1:p.Glu1212Val
XR_002956289.1:n.4027A>T
NM_001363725.2:c.1484A>T	NP_001350654.1:p.Glu495Val
NM_001371656.1:c.3863A>T	NP_001358585.1:p.Glu1288Val
NM_001374820.1:c.3863A>T	NP_001361749.1:p.Glu1288Val
NM_001374828.1:c.3983A>T MANE Select	NP_001361757.1:p.Glu1328Val
NM_017519.3:c.3824A>T	NP_059989.3:p.Glu1275Val