Canonical Allele Identifier: CA366227554

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181049G>A , CM000668.2:g.157181049G>A	GRCh38
NC_000006.11:g.157502183G>A , CM000668.1:g.157502183G>A	GRCh37
NC_000006.10:g.157543875G>A	NCBI36
NG_032093.1:g.408120G>A
NG_032093.2:g.408120G>A
NG_066624.1:g.410024G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.3585G>A MANE Select	NP_001361757.1:p.Trp1195Ter
ENST00000636930.2:c.3585G>A MANE Select	ENSP00000490491.2:p.Trp1195Ter
NM_001346813.1:c.3336G>A	NP_001333742.1:p.Trp1112Ter
NM_001363725.1:c.1086G>A	NP_001350654.1:p.Trp362Ter
NM_001363725.2:c.1086G>A	NP_001350654.1:p.Trp362Ter
NM_001371656.1:c.3465G>A	NP_001358585.1:p.Trp1155Ter
NM_001374820.1:c.3465G>A	NP_001361749.1:p.Trp1155Ter
NM_017519.2:c.3177G>A	NP_059989.2:p.Trp1059Ter
NM_017519.3:c.3426G>A	NP_059989.3:p.Trp1142Ter
NM_020732.3:c.3216G>A	NP_065783.3:p.Trp1072Ter
ENST00000319584.10:c.1602G>A	ENSP00000313006.6:p.Trp534Ter
ENST00000319584.11:c.1599G>A	ENSP00000313006.7:p.Trp533Ter
ENST00000346085.10:c.3465G>A	ENSP00000344546.5:p.Trp1155Ter
ENST00000346085.9:c.3216G>A	ENSP00000344546.4:p.Trp1072Ter
ENST00000350026.10:c.3177G>A	ENSP00000055163.7:p.Trp1059Ter
ENST00000350026.11:c.3426G>A	ENSP00000055163.8:p.Trp1142Ter
ENST00000350026.9:c.3177G>A	ENSP00000055163.7:p.Trp1059Ter
ENST00000400790.3:c.378G>A	ENSP00000383596.3:p.Trp126Ter
ENST00000414678.6:c.1743G>A	ENSP00000412835.2:p.Trp581Ter
ENST00000414678.7:c.1743G>A	ENSP00000412835.2:p.Trp581Ter
ENST00000414678.8:c.3495G>A	ENSP00000412835.3:p.Trp1165Ter
ENST00000478761.3:c.787G>A
ENST00000635849.1:c.906G>A	ENSP00000490948.1:p.Trp302Ter
ENST00000635957.1:c.540G>A	ENSP00000490385.1:p.Trp180Ter
ENST00000636940.1:n.1582G>A
ENST00000637015.1:c.953G>A
ENST00000637015.2:c.3714G>A	ENSP00000489729.2:p.Trp1238Ter
ENST00000637568.1:c.867G>A
ENST00000637741.1:n.251G>A
ENST00000637810.1:c.927G>A	ENSP00000489636.1:p.Trp309Ter
ENST00000637904.1:c.1086G>A	ENSP00000490550.1:p.Trp362Ter
ENST00000647938.1:c.3216G>A	ENSP00000498155.1:p.Trp1072Ter
XM_005267069.3:c.3336G>A	XP_005267126.2:p.Trp1112Ter
XM_011535984.1:c.2415G>A	XP_011534286.1:p.Trp805Ter
XM_011535984.2:c.3546G>A	XP_011534286.2:p.Trp1182Ter
XM_011535985.1:c.2235G>A	XP_011534287.1:p.Trp745Ter
XM_011535986.1:c.1995G>A	XP_011534288.1:p.Trp665Ter
XM_011535987.1:c.1614G>A	XP_011534289.1:p.Trp538Ter
XM_011535988.1:c.477G>A	XP_011534290.1:p.Trp159Ter
XM_011535988.3:c.477G>A	XP_011534290.1:p.Trp159Ter
XM_017011103.2:c.3447G>A	XP_016866592.1:p.Trp1149Ter
XM_017011104.1:c.3417G>A	XP_016866593.1:p.Trp1139Ter
XM_017011105.2:c.3387G>A	XP_016866594.1:p.Trp1129Ter
XM_017011106.2:c.3258G>A	XP_016866595.1:p.Trp1086Ter
XM_017011107.2:c.3237G>A	XP_016866596.1:p.Trp1079Ter
XR_002956289.1:n.3629G>A