Canonical Allele Identifier: CA4067749

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 589098
• ClinVar RCV Id: RCV001816773 ; RCV002318040 ; RCV003574805
• dbSNP Id: rs776881575
• ExAC: 6:157522387 G / A
• gnomAD v2: 6-157522387-G-A
• gnomAD v3: 6-157201253-G-A
• gnomAD v4: 6-157201253-G-A
• MyVariant Identifiers: chr6:g.157522387G>A (hg19) ; chr6:g.157201253G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201253G>A , CM000668.2:g.157201253G>A	GRCh38
NC_000006.11:g.157522387G>A , CM000668.1:g.157522387G>A	GRCh37
NC_000006.10:g.157564079G>A	NCBI36
NG_032093.1:g.428324G>A
NG_032093.2:g.428324G>A
NG_066624.1:g.430228G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4869G>A	ENSP00000055163.8:p.Ala1623=
ENST00000414678.8:c.4938G>A	ENSP00000412835.3:p.Ala1646=
ENST00000637015.2:c.5157G>A	ENSP00000489729.2:p.Ala1719=
ENST00000346085.10:c.4908G>A	ENSP00000344546.5:p.Ala1636=
ENST00000350026.10:c.4620G>A	ENSP00000055163.7:p.Ala1540=
ENST00000414678.7:c.3186G>A	ENSP00000412835.2:p.Ala1062=
ENST00000635849.1:c.2349G>A	ENSP00000490948.1:p.Ala783=
ENST00000635957.1:c.1980G>A	ENSP00000490385.1:p.Ala660=
ENST00000636227.1:n.3491G>A
ENST00000636254.1:n.948G>A
ENST00000636930.2:c.5028G>A MANE Select	ENSP00000490491.2:p.Ala1676=
ENST00000636940.1:n.3025G>A
ENST00000637015.1:c.2396G>A
ENST00000637568.1:c.2310G>A
ENST00000637741.1:n.1694G>A
ENST00000637810.1:c.2370G>A	ENSP00000489636.1:p.Ala790=
ENST00000637904.1:c.2529G>A	ENSP00000490550.1:p.Ala843=
ENST00000647938.1:c.4659G>A	ENSP00000498155.1:p.Ala1553=
ENST00000346085.9:c.4659G>A	ENSP00000344546.4:p.Ala1553=
ENST00000350026.9:c.4620G>A	ENSP00000055163.7:p.Ala1540=
ENST00000414678.6:c.3186G>A	ENSP00000412835.2:p.Ala1062=
NM_017519.2:c.4620G>A	NP_059989.2:p.Ala1540=
NM_020732.3:c.4659G>A	NP_065783.3:p.Ala1553=
XM_005267069.3:c.4779G>A	XP_005267126.2:p.Ala1593=
XM_011535984.1:c.3858G>A	XP_011534286.1:p.Ala1286=
XM_011535985.1:c.3678G>A	XP_011534287.1:p.Ala1226=
XM_011535986.1:c.3438G>A	XP_011534288.1:p.Ala1146=
XM_011535987.1:c.3057G>A	XP_011534289.1:p.Ala1019=
XM_011535988.1:c.1920G>A	XP_011534290.1:p.Ala640=
NM_001346813.1:c.4779G>A	NP_001333742.1:p.Ala1593=
NM_001363725.1:c.2529G>A	NP_001350654.1:p.Ala843=
XM_011535984.2:c.4989G>A	XP_011534286.2:p.Ala1663=
XM_011535988.3:c.1920G>A	XP_011534290.1:p.Ala640=
XM_017011103.2:c.4890G>A	XP_016866592.1:p.Ala1630=
XM_017011104.1:c.4860G>A	XP_016866593.1:p.Ala1620=
XM_017011105.2:c.4830G>A	XP_016866594.1:p.Ala1610=
XM_017011106.2:c.4701G>A	XP_016866595.1:p.Ala1567=
XM_017011107.2:c.4680G>A	XP_016866596.1:p.Ala1560=
XR_002956289.1:n.4975G>A
NM_001363725.2:c.2529G>A	NP_001350654.1:p.Ala843=
NM_001371656.1:c.4908G>A	NP_001358585.1:p.Ala1636=
NM_001374820.1:c.4908G>A	NP_001361749.1:p.Ala1636=
NM_001374828.1:c.5028G>A MANE Select	NP_001361757.1:p.Ala1676=
NM_017519.3:c.4869G>A	NP_059989.3:p.Ala1623=