Canonical Allele Identifier: CA4067740

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1960419
• ClinVar RCV Id: RCV002706473
• dbSNP Id: rs542516057
• ExAC: 6:157522328 C / T
• gnomAD v2: 6-157522328-C-T
• gnomAD v3: 6-157201194-C-T
• gnomAD v4: 6-157201194-C-T
• MyVariant Identifiers: chr6:g.157522328C>T (hg19) ; chr6:g.157201194C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201194C>T , CM000668.2:g.157201194C>T	GRCh38
NC_000006.11:g.157522328C>T , CM000668.1:g.157522328C>T	GRCh37
NC_000006.10:g.157564020C>T	NCBI36
NG_032093.1:g.428265C>T
NG_032093.2:g.428265C>T
NG_066624.1:g.430169C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4810C>T	ENSP00000055163.8:p.Arg1604Cys
ENST00000414678.8:c.4879C>T	ENSP00000412835.3:p.Arg1627Cys
ENST00000637015.2:c.5098C>T	ENSP00000489729.2:p.Arg1700Cys
ENST00000346085.10:c.4849C>T	ENSP00000344546.5:p.Arg1617Cys
ENST00000350026.10:c.4561C>T	ENSP00000055163.7:p.Arg1521Cys
ENST00000414678.7:c.3127C>T	ENSP00000412835.2:p.Arg1043Cys
ENST00000635849.1:c.2290C>T	ENSP00000490948.1:p.Arg764Cys
ENST00000635957.1:c.1921C>T	ENSP00000490385.1:p.Arg641Cys
ENST00000636227.1:n.3432C>T
ENST00000636254.1:n.889C>T
ENST00000636930.2:c.4969C>T MANE Select	ENSP00000490491.2:p.Arg1657Cys
ENST00000636940.1:n.2966C>T
ENST00000637015.1:c.2337C>T
ENST00000637568.1:c.2251C>T
ENST00000637741.1:n.1635C>T
ENST00000637810.1:c.2311C>T	ENSP00000489636.1:p.Arg771Cys
ENST00000637904.1:c.2470C>T	ENSP00000490550.1:p.Arg824Cys
ENST00000647938.1:c.4600C>T	ENSP00000498155.1:p.Arg1534Cys
ENST00000346085.9:c.4600C>T	ENSP00000344546.4:p.Arg1534Cys
ENST00000350026.9:c.4561C>T	ENSP00000055163.7:p.Arg1521Cys
ENST00000414678.6:c.3127C>T	ENSP00000412835.2:p.Arg1043Cys
NM_017519.2:c.4561C>T	NP_059989.2:p.Arg1521Cys
NM_020732.3:c.4600C>T	NP_065783.3:p.Arg1534Cys
XM_005267069.3:c.4720C>T	XP_005267126.2:p.Arg1574Cys
XM_011535984.1:c.3799C>T	XP_011534286.1:p.Arg1267Cys
XM_011535985.1:c.3619C>T	XP_011534287.1:p.Arg1207Cys
XM_011535986.1:c.3379C>T	XP_011534288.1:p.Arg1127Cys
XM_011535987.1:c.2998C>T	XP_011534289.1:p.Arg1000Cys
XM_011535988.1:c.1861C>T	XP_011534290.1:p.Arg621Cys
NM_001346813.1:c.4720C>T	NP_001333742.1:p.Arg1574Cys
NM_001363725.1:c.2470C>T	NP_001350654.1:p.Arg824Cys
XM_011535984.2:c.4930C>T	XP_011534286.2:p.Arg1644Cys
XM_011535988.3:c.1861C>T	XP_011534290.1:p.Arg621Cys
XM_017011103.2:c.4831C>T	XP_016866592.1:p.Arg1611Cys
XM_017011104.1:c.4801C>T	XP_016866593.1:p.Arg1601Cys
XM_017011105.2:c.4771C>T	XP_016866594.1:p.Arg1591Cys
XM_017011106.2:c.4642C>T	XP_016866595.1:p.Arg1548Cys
XM_017011107.2:c.4621C>T	XP_016866596.1:p.Arg1541Cys
XR_002956289.1:n.4916C>T
NM_001363725.2:c.2470C>T	NP_001350654.1:p.Arg824Cys
NM_001371656.1:c.4849C>T	NP_001358585.1:p.Arg1617Cys
NM_001374820.1:c.4849C>T	NP_001361749.1:p.Arg1617Cys
NM_001374828.1:c.4969C>T MANE Select	NP_001361757.1:p.Arg1657Cys
NM_017519.3:c.4810C>T	NP_059989.3:p.Arg1604Cys