Canonical Allele Identifier: CA366234089

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338804
• MyVariant Identifiers: chr6:g.157510823A>T (hg19) ; chr6:g.157189689A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189689A>T , CM000668.2:g.157189689A>T	GRCh38
NC_000006.11:g.157510823A>T , CM000668.1:g.157510823A>T	GRCh37
NC_000006.10:g.157552515A>T	NCBI36
NG_032093.1:g.416760A>T
NG_032093.2:g.416760A>T
NG_066624.1:g.418664A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3808A>T	ENSP00000055163.8:p.Ser1270Cys
ENST00000414678.8:c.3877A>T	ENSP00000412835.3:p.Ser1293Cys
ENST00000637015.2:c.4096A>T	ENSP00000489729.2:p.Ser1366Cys
ENST00000346085.10:c.3847A>T	ENSP00000344546.5:p.Ser1283Cys
ENST00000350026.10:c.3559A>T	ENSP00000055163.7:p.Ser1187Cys
ENST00000414678.7:c.2125A>T	ENSP00000412835.2:p.Ser709Cys
ENST00000635849.1:c.1288A>T	ENSP00000490948.1:p.Ser430Cys
ENST00000635957.1:c.922A>T	ENSP00000490385.1:p.Ser308Cys
ENST00000636930.2:c.3967A>T MANE Select	ENSP00000490491.2:p.Ser1323Cys
ENST00000636940.1:n.1964A>T
ENST00000637015.1:c.1335A>T
ENST00000637568.1:c.1249A>T
ENST00000637741.1:n.633A>T
ENST00000637810.1:c.1309A>T	ENSP00000489636.1:p.Ser437Cys
ENST00000637904.1:c.1468A>T	ENSP00000490550.1:p.Ser490Cys
ENST00000647938.1:c.3598A>T	ENSP00000498155.1:p.Ser1200Cys
ENST00000346085.9:c.3598A>T	ENSP00000344546.4:p.Ser1200Cys
ENST00000350026.9:c.3559A>T	ENSP00000055163.7:p.Ser1187Cys
ENST00000414678.6:c.2125A>T	ENSP00000412835.2:p.Ser709Cys
NM_017519.2:c.3559A>T	NP_059989.2:p.Ser1187Cys
NM_020732.3:c.3598A>T	NP_065783.3:p.Ser1200Cys
XM_005267069.3:c.3718A>T	XP_005267126.2:p.Ser1240Cys
XM_011535984.1:c.2797A>T	XP_011534286.1:p.Ser933Cys
XM_011535985.1:c.2617A>T	XP_011534287.1:p.Ser873Cys
XM_011535986.1:c.2377A>T	XP_011534288.1:p.Ser793Cys
XM_011535987.1:c.1996A>T	XP_011534289.1:p.Ser666Cys
XM_011535988.1:c.859A>T	XP_011534290.1:p.Ser287Cys
NM_001346813.1:c.3718A>T	NP_001333742.1:p.Ser1240Cys
NM_001363725.1:c.1468A>T	NP_001350654.1:p.Ser490Cys
XM_011535984.2:c.3928A>T	XP_011534286.2:p.Ser1310Cys
XM_011535988.3:c.859A>T	XP_011534290.1:p.Ser287Cys
XM_017011103.2:c.3829A>T	XP_016866592.1:p.Ser1277Cys
XM_017011104.1:c.3799A>T	XP_016866593.1:p.Ser1267Cys
XM_017011105.2:c.3769A>T	XP_016866594.1:p.Ser1257Cys
XM_017011106.2:c.3640A>T	XP_016866595.1:p.Ser1214Cys
XM_017011107.2:c.3619A>T	XP_016866596.1:p.Ser1207Cys
XR_002956289.1:n.4011A>T
NM_001363725.2:c.1468A>T	NP_001350654.1:p.Ser490Cys
NM_001371656.1:c.3847A>T	NP_001358585.1:p.Ser1283Cys
NM_001374820.1:c.3847A>T	NP_001361749.1:p.Ser1283Cys
NM_001374828.1:c.3967A>T MANE Select	NP_001361757.1:p.Ser1323Cys
NM_017519.3:c.3808A>T	NP_059989.3:p.Ser1270Cys