Canonical Allele Identifier: CA2573052638

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1319701
• ClinVar RCV Id: RCV003237689
• dbSNP Id: rs2128339720

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190104dup , CM000668.2:g.157190104dup	GRCh38
NC_000006.11:g.157511238dup , CM000668.1:g.157511238dup	GRCh37
NC_000006.10:g.157552930dup	NCBI36
NG_032093.1:g.417175dup
NG_032093.2:g.417175dup
NG_066624.1:g.419079dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3966dup	ENSP00000055163.8:p.Ser1323LeufsTer24
ENST00000414678.8:c.4035dup	ENSP00000412835.3:p.Ser1346LeufsTer24
ENST00000637015.2:c.4254dup	ENSP00000489729.2:p.Ser1419LeufsTer24
ENST00000346085.10:c.4005dup	ENSP00000344546.5:p.Ser1336LeufsTer24
ENST00000350026.10:c.3717dup	ENSP00000055163.7:p.Ser1240LeufsTer24
ENST00000414678.7:c.2283dup	ENSP00000412835.2:p.Ser762LeufsTer24
ENST00000635849.1:c.1446dup	ENSP00000490948.1:p.Ser483LeufsTer24
ENST00000635957.1:c.1077dup	ENSP00000490385.1:p.Ser360LeufsTer24
ENST00000636930.2:c.4125dup MANE Select	ENSP00000490491.2:p.Ser1376LeufsTer24
ENST00000636940.1:n.2122dup
ENST00000637015.1:c.1493dup
ENST00000637568.1:c.1407dup
ENST00000637741.1:n.791dup
ENST00000637810.1:c.1467dup	ENSP00000489636.1:p.Ser490LeufsTer24
ENST00000637904.1:c.1626dup	ENSP00000490550.1:p.Ser543LeufsTer24
ENST00000647938.1:c.3756dup	ENSP00000498155.1:p.Ser1253LeufsTer24
ENST00000346085.9:c.3756dup	ENSP00000344546.4:p.Ser1253LeufsTer24
ENST00000350026.9:c.3717dup	ENSP00000055163.7:p.Ser1240LeufsTer24
ENST00000414678.6:c.2283dup	ENSP00000412835.2:p.Ser762LeufsTer24
NM_017519.2:c.3717dup	NP_059989.2:p.Ser1240LeufsTer24
NM_020732.3:c.3756dup	NP_065783.3:p.Ser1253LeufsTer24
XM_005267069.3:c.3876dup	XP_005267126.2:p.Ser1293LeufsTer24
XM_011535984.1:c.2955dup	XP_011534286.1:p.Ser986LeufsTer24
XM_011535985.1:c.2775dup	XP_011534287.1:p.Ser926LeufsTer24
XM_011535986.1:c.2535dup	XP_011534288.1:p.Ser846LeufsTer24
XM_011535987.1:c.2154dup	XP_011534289.1:p.Ser719LeufsTer24
XM_011535988.1:c.1017dup	XP_011534290.1:p.Ser340LeufsTer24
NM_001346813.1:c.3876dup	NP_001333742.1:p.Ser1293LeufsTer24
NM_001363725.1:c.1626dup	NP_001350654.1:p.Ser543LeufsTer24
XM_011535984.2:c.4086dup	XP_011534286.2:p.Ser1363LeufsTer24
XM_011535988.3:c.1017dup	XP_011534290.1:p.Ser340LeufsTer24
XM_017011103.2:c.3987dup	XP_016866592.1:p.Ser1330LeufsTer24
XM_017011104.1:c.3957dup	XP_016866593.1:p.Ser1320LeufsTer24
XM_017011105.2:c.3927dup	XP_016866594.1:p.Ser1310LeufsTer24
XM_017011106.2:c.3798dup	XP_016866595.1:p.Ser1267LeufsTer24
XM_017011107.2:c.3777dup	XP_016866596.1:p.Ser1260LeufsTer24
XR_002956289.1:n.4169dup
NM_001363725.2:c.1626dup	NP_001350654.1:p.Ser543LeufsTer24
NM_001371656.1:c.4005dup	NP_001358585.1:p.Ser1336LeufsTer24
NM_001374820.1:c.4005dup	NP_001361749.1:p.Ser1336LeufsTer24
NM_001374828.1:c.4125dup MANE Select	NP_001361757.1:p.Ser1376LeufsTer24
NM_017519.3:c.3966dup	NP_059989.3:p.Ser1323LeufsTer24