Canonical Allele Identifier: CA452784838

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1337282
• ClinVar RCV Id: RCV001820296
• dbSNP Id: rs1197819486
• gnomAD v3: 6-157201397-A-G
• gnomAD v4: 6-157201397-A-G
• MyVariant Identifiers: chr6:g.157522531A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201397A>G , CM000668.2:g.157201397A>G	GRCh38
NC_000006.11:g.157522531A>G , CM000668.1:g.157522531A>G	GRCh37
NC_000006.10:g.157564223A>G	NCBI36
NG_032093.1:g.428468A>G
NG_032093.2:g.428468A>G
NG_066624.1:g.430372A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5013A>G	ENSP00000055163.8:p.Pro1671=
ENST00000414678.8:c.5082A>G	ENSP00000412835.3:p.Pro1694=
ENST00000637015.2:c.5301A>G	ENSP00000489729.2:p.Pro1767=
ENST00000346085.10:c.5052A>G	ENSP00000344546.5:p.Pro1684=
ENST00000350026.10:c.4764A>G	ENSP00000055163.7:p.Pro1588=
ENST00000414678.7:c.3330A>G	ENSP00000412835.2:p.Pro1110=
ENST00000635849.1:c.2493A>G	ENSP00000490948.1:p.Pro831=
ENST00000635957.1:c.2124A>G	ENSP00000490385.1:p.Pro708=
ENST00000636227.1:n.3635A>G
ENST00000636254.1:n.1092A>G
ENST00000636930.2:c.5172A>G MANE Select	ENSP00000490491.2:p.Pro1724=
ENST00000636940.1:n.3169A>G
ENST00000637015.1:c.2540A>G
ENST00000637568.1:c.2454A>G
ENST00000637741.1:n.1838A>G
ENST00000637810.1:c.2514A>G	ENSP00000489636.1:p.Pro838=
ENST00000637904.1:c.2673A>G	ENSP00000490550.1:p.Pro891=
ENST00000647938.1:c.4803A>G	ENSP00000498155.1:p.Pro1601=
ENST00000346085.9:c.4803A>G	ENSP00000344546.4:p.Pro1601=
ENST00000350026.9:c.4764A>G	ENSP00000055163.7:p.Pro1588=
ENST00000414678.6:c.3330A>G	ENSP00000412835.2:p.Pro1110=
NM_017519.2:c.4764A>G	NP_059989.2:p.Pro1588=
NM_020732.3:c.4803A>G	NP_065783.3:p.Pro1601=
XM_005267069.3:c.4923A>G	XP_005267126.2:p.Pro1641=
XM_011535984.1:c.4002A>G	XP_011534286.1:p.Pro1334=
XM_011535985.1:c.3822A>G	XP_011534287.1:p.Pro1274=
XM_011535986.1:c.3582A>G	XP_011534288.1:p.Pro1194=
XM_011535987.1:c.3201A>G	XP_011534289.1:p.Pro1067=
XM_011535988.1:c.2064A>G	XP_011534290.1:p.Pro688=
NM_001346813.1:c.4923A>G	NP_001333742.1:p.Pro1641=
NM_001363725.1:c.2673A>G	NP_001350654.1:p.Pro891=
XM_011535984.2:c.5133A>G	XP_011534286.2:p.Pro1711=
XM_011535988.3:c.2064A>G	XP_011534290.1:p.Pro688=
XM_017011103.2:c.5034A>G	XP_016866592.1:p.Pro1678=
XM_017011104.1:c.5004A>G	XP_016866593.1:p.Pro1668=
XM_017011105.2:c.4974A>G	XP_016866594.1:p.Pro1658=
XM_017011106.2:c.4845A>G	XP_016866595.1:p.Pro1615=
XM_017011107.2:c.4824A>G	XP_016866596.1:p.Pro1608=
XR_002956289.1:n.5119A>G
NM_001363725.2:c.2673A>G	NP_001350654.1:p.Pro891=
NM_001371656.1:c.5052A>G	NP_001358585.1:p.Pro1684=
NM_001374820.1:c.5052A>G	NP_001361749.1:p.Pro1684=
NM_001374828.1:c.5172A>G MANE Select	NP_001361757.1:p.Pro1724=
NM_017519.3:c.5013A>G	NP_059989.3:p.Pro1671=