Canonical Allele Identifier: CA366241128

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1710708
• ClinVar RCV Id: RCV002291995
• gnomAD v4: 6-157200876-A-G
• MyVariant Identifiers: chr6:g.157522010A>G (hg19) ; chr6:g.157200876A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200876A>G , CM000668.2:g.157200876A>G	GRCh38
NC_000006.11:g.157522010A>G , CM000668.1:g.157522010A>G	GRCh37
NC_000006.10:g.157563702A>G	NCBI36
NG_032093.1:g.427947A>G
NG_032093.2:g.427947A>G
NG_066624.1:g.429851A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4492A>G	ENSP00000055163.8:p.Ser1498Gly
ENST00000414678.8:c.4561A>G	ENSP00000412835.3:p.Ser1521Gly
ENST00000637015.2:c.4780A>G	ENSP00000489729.2:p.Ser1594Gly
ENST00000346085.10:c.4531A>G	ENSP00000344546.5:p.Ser1511Gly
ENST00000350026.10:c.4243A>G	ENSP00000055163.7:p.Ser1415Gly
ENST00000414678.7:c.2809A>G	ENSP00000412835.2:p.Ser937Gly
ENST00000635849.1:c.1972A>G	ENSP00000490948.1:p.Ser658Gly
ENST00000635957.1:c.1603A>G	ENSP00000490385.1:p.Ser535Gly
ENST00000636227.1:n.3114A>G
ENST00000636254.1:n.571A>G
ENST00000636930.2:c.4651A>G MANE Select	ENSP00000490491.2:p.Ser1551Gly
ENST00000636940.1:n.2648A>G
ENST00000637015.1:c.2019A>G
ENST00000637568.1:c.1933A>G
ENST00000637741.1:n.1317A>G
ENST00000637810.1:c.1993A>G	ENSP00000489636.1:p.Ser665Gly
ENST00000637904.1:c.2152A>G	ENSP00000490550.1:p.Ser718Gly
ENST00000647938.1:c.4282A>G	ENSP00000498155.1:p.Ser1428Gly
ENST00000346085.9:c.4282A>G	ENSP00000344546.4:p.Ser1428Gly
ENST00000350026.9:c.4243A>G	ENSP00000055163.7:p.Ser1415Gly
ENST00000414678.6:c.2809A>G	ENSP00000412835.2:p.Ser937Gly
NM_017519.2:c.4243A>G	NP_059989.2:p.Ser1415Gly
NM_020732.3:c.4282A>G	NP_065783.3:p.Ser1428Gly
XM_005267069.3:c.4402A>G	XP_005267126.2:p.Ser1468Gly
XM_011535984.1:c.3481A>G	XP_011534286.1:p.Ser1161Gly
XM_011535985.1:c.3301A>G	XP_011534287.1:p.Ser1101Gly
XM_011535986.1:c.3061A>G	XP_011534288.1:p.Ser1021Gly
XM_011535987.1:c.2680A>G	XP_011534289.1:p.Ser894Gly
XM_011535988.1:c.1543A>G	XP_011534290.1:p.Ser515Gly
NM_001346813.1:c.4402A>G	NP_001333742.1:p.Ser1468Gly
NM_001363725.1:c.2152A>G	NP_001350654.1:p.Ser718Gly
XM_011535984.2:c.4612A>G	XP_011534286.2:p.Ser1538Gly
XM_011535988.3:c.1543A>G	XP_011534290.1:p.Ser515Gly
XM_017011103.2:c.4513A>G	XP_016866592.1:p.Ser1505Gly
XM_017011104.1:c.4483A>G	XP_016866593.1:p.Ser1495Gly
XM_017011105.2:c.4453A>G	XP_016866594.1:p.Ser1485Gly
XM_017011106.2:c.4324A>G	XP_016866595.1:p.Ser1442Gly
XM_017011107.2:c.4303A>G	XP_016866596.1:p.Ser1435Gly
XR_002956289.1:n.4598A>G
NM_001363725.2:c.2152A>G	NP_001350654.1:p.Ser718Gly
NM_001371656.1:c.4531A>G	NP_001358585.1:p.Ser1511Gly
NM_001374820.1:c.4531A>G	NP_001361749.1:p.Ser1511Gly
NM_001374828.1:c.4651A>G MANE Select	NP_001361757.1:p.Ser1551Gly
NM_017519.3:c.4492A>G	NP_059989.3:p.Ser1498Gly