Canonical Allele Identifier: CA2573052636

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1323927
• ClinVar RCV Id: RCV001785960
• dbSNP Id: rs2128317569

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181128dup , CM000668.2:g.157181128dup	GRCh38
NC_000006.11:g.157502262dup , CM000668.1:g.157502262dup	GRCh37
NC_000006.10:g.157543954dup	NCBI36
NG_032093.1:g.408199dup
NG_032093.2:g.408199dup
NG_066624.1:g.410103dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3505dup	ENSP00000055163.8:p.Asp1169GlyfsTer19
ENST00000414678.8:c.3574dup	ENSP00000412835.3:p.Asp1192GlyfsTer19
ENST00000637015.2:c.3793dup	ENSP00000489729.2:p.Asp1265GlyfsTer19
ENST00000319584.11:c.1678dup	ENSP00000313006.7:p.Asp560GlyfsTer19
ENST00000346085.10:c.3544dup	ENSP00000344546.5:p.Asp1182GlyfsTer19
ENST00000350026.10:c.3256dup	ENSP00000055163.7:p.Asp1086GlyfsTer19
ENST00000414678.7:c.1822dup	ENSP00000412835.2:p.Asp608GlyfsTer19
ENST00000635849.1:c.985dup	ENSP00000490948.1:p.Asp329GlyfsTer19
ENST00000635957.1:c.619dup	ENSP00000490385.1:p.Asp207GlyfsTer19
ENST00000636930.2:c.3664dup MANE Select	ENSP00000490491.2:p.Asp1222GlyfsTer19
ENST00000636940.1:n.1661dup
ENST00000637015.1:c.1032dup
ENST00000637568.1:c.946dup
ENST00000637741.1:n.330dup
ENST00000637810.1:c.1006dup	ENSP00000489636.1:p.Asp336GlyfsTer19
ENST00000637904.1:c.1165dup	ENSP00000490550.1:p.Asp389GlyfsTer19
ENST00000647938.1:c.3295dup	ENSP00000498155.1:p.Asp1099GlyfsTer19
ENST00000319584.10:c.1681dup	ENSP00000313006.6:p.Asp561GlyfsTer19
ENST00000346085.9:c.3295dup	ENSP00000344546.4:p.Asp1099GlyfsTer19
ENST00000350026.9:c.3256dup	ENSP00000055163.7:p.Asp1086GlyfsTer19
ENST00000400790.3:c.457dup	ENSP00000383596.3:p.Asp153GlyfsTer19
ENST00000414678.6:c.1822dup	ENSP00000412835.2:p.Asp608GlyfsTer19
ENST00000478761.3:c.866dup
NM_017519.2:c.3256dup	NP_059989.2:p.Asp1086GlyfsTer19
NM_020732.3:c.3295dup	NP_065783.3:p.Asp1099GlyfsTer19
XM_005267069.3:c.3415dup	XP_005267126.2:p.Asp1139GlyfsTer19
XM_011535984.1:c.2494dup	XP_011534286.1:p.Asp832GlyfsTer19
XM_011535985.1:c.2314dup	XP_011534287.1:p.Asp772GlyfsTer19
XM_011535986.1:c.2074dup	XP_011534288.1:p.Asp692GlyfsTer19
XM_011535987.1:c.1693dup	XP_011534289.1:p.Asp565GlyfsTer19
XM_011535988.1:c.556dup	XP_011534290.1:p.Asp186GlyfsTer19
NM_001346813.1:c.3415dup	NP_001333742.1:p.Asp1139GlyfsTer19
NM_001363725.1:c.1165dup	NP_001350654.1:p.Asp389GlyfsTer19
XM_011535984.2:c.3625dup	XP_011534286.2:p.Asp1209GlyfsTer19
XM_011535988.3:c.556dup	XP_011534290.1:p.Asp186GlyfsTer19
XM_017011103.2:c.3526dup	XP_016866592.1:p.Asp1176GlyfsTer19
XM_017011104.1:c.3496dup	XP_016866593.1:p.Asp1166GlyfsTer19
XM_017011105.2:c.3466dup	XP_016866594.1:p.Asp1156GlyfsTer19
XM_017011106.2:c.3337dup	XP_016866595.1:p.Asp1113GlyfsTer19
XM_017011107.2:c.3316dup	XP_016866596.1:p.Asp1106GlyfsTer19
XR_002956289.1:n.3708dup
NM_001363725.2:c.1165dup	NP_001350654.1:p.Asp389GlyfsTer19
NM_001371656.1:c.3544dup	NP_001358585.1:p.Asp1182GlyfsTer19
NM_001374820.1:c.3544dup	NP_001361749.1:p.Asp1182GlyfsTer19
NM_001374828.1:c.3664dup MANE Select	NP_001361757.1:p.Asp1222GlyfsTer19
NM_017519.3:c.3505dup	NP_059989.3:p.Asp1169GlyfsTer19