Canonical Allele Identifier: CA366234576

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511173A>T (hg19) ; chr6:g.157190039A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190039A>T , CM000668.2:g.157190039A>T	GRCh38
NC_000006.11:g.157511173A>T , CM000668.1:g.157511173A>T	GRCh37
NC_000006.10:g.157552865A>T	NCBI36
NG_032093.1:g.417110A>T
NG_032093.2:g.417110A>T
NG_066624.1:g.419014A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3901A>T	ENSP00000055163.8:p.Ser1301Cys
ENST00000414678.8:c.3970A>T	ENSP00000412835.3:p.Ser1324Cys
ENST00000637015.2:c.4189A>T	ENSP00000489729.2:p.Ser1397Cys
ENST00000346085.10:c.3940A>T	ENSP00000344546.5:p.Ser1314Cys
ENST00000350026.10:c.3652A>T	ENSP00000055163.7:p.Ser1218Cys
ENST00000414678.7:c.2218A>T	ENSP00000412835.2:p.Ser740Cys
ENST00000635849.1:c.1381A>T	ENSP00000490948.1:p.Ser461Cys
ENST00000635957.1:c.1014-2A>T	ENSP00000490385.1:n.1014-2A>T
ENST00000636930.2:c.4060A>T MANE Select	ENSP00000490491.2:p.Ser1354Cys
ENST00000636940.1:n.2057A>T
ENST00000637015.1:c.1428A>T
ENST00000637568.1:c.1342A>T
ENST00000637741.1:n.726A>T
ENST00000637810.1:c.1402A>T	ENSP00000489636.1:p.Ser468Cys
ENST00000637904.1:c.1561A>T	ENSP00000490550.1:p.Ser521Cys
ENST00000647938.1:c.3691A>T	ENSP00000498155.1:p.Ser1231Cys
ENST00000346085.9:c.3691A>T	ENSP00000344546.4:p.Ser1231Cys
ENST00000350026.9:c.3652A>T	ENSP00000055163.7:p.Ser1218Cys
ENST00000414678.6:c.2218A>T	ENSP00000412835.2:p.Ser740Cys
NM_017519.2:c.3652A>T	NP_059989.2:p.Ser1218Cys
NM_020732.3:c.3691A>T	NP_065783.3:p.Ser1231Cys
XM_005267069.3:c.3811A>T	XP_005267126.2:p.Ser1271Cys
XM_011535984.1:c.2890A>T	XP_011534286.1:p.Ser964Cys
XM_011535985.1:c.2710A>T	XP_011534287.1:p.Ser904Cys
XM_011535986.1:c.2470A>T	XP_011534288.1:p.Ser824Cys
XM_011535987.1:c.2089A>T	XP_011534289.1:p.Ser697Cys
XM_011535988.1:c.952A>T	XP_011534290.1:p.Ser318Cys
NM_001346813.1:c.3811A>T	NP_001333742.1:p.Ser1271Cys
NM_001363725.1:c.1561A>T	NP_001350654.1:p.Ser521Cys
XM_011535984.2:c.4021A>T	XP_011534286.2:p.Ser1341Cys
XM_011535988.3:c.952A>T	XP_011534290.1:p.Ser318Cys
XM_017011103.2:c.3922A>T	XP_016866592.1:p.Ser1308Cys
XM_017011104.1:c.3892A>T	XP_016866593.1:p.Ser1298Cys
XM_017011105.2:c.3862A>T	XP_016866594.1:p.Ser1288Cys
XM_017011106.2:c.3733A>T	XP_016866595.1:p.Ser1245Cys
XM_017011107.2:c.3712A>T	XP_016866596.1:p.Ser1238Cys
XR_002956289.1:n.4104A>T
NM_001363725.2:c.1561A>T	NP_001350654.1:p.Ser521Cys
NM_001371656.1:c.3940A>T	NP_001358585.1:p.Ser1314Cys
NM_001374820.1:c.3940A>T	NP_001361749.1:p.Ser1314Cys
NM_001374828.1:c.4060A>T MANE Select	NP_001361757.1:p.Ser1354Cys
NM_017519.3:c.3901A>T	NP_059989.3:p.Ser1301Cys