Canonical Allele Identifier: CA452978367

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201343-C-G
• MyVariant Identifiers: chr6:g.157522477C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201343C>G , CM000668.2:g.157201343C>G	GRCh38
NC_000006.11:g.157522477C>G , CM000668.1:g.157522477C>G	GRCh37
NC_000006.10:g.157564169C>G	NCBI36
NG_032093.1:g.428414C>G
NG_032093.2:g.428414C>G
NG_066624.1:g.430318C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4959C>G	ENSP00000055163.8:p.Val1653=
ENST00000414678.8:c.5028C>G	ENSP00000412835.3:p.Val1676=
ENST00000637015.2:c.5247C>G	ENSP00000489729.2:p.Val1749=
ENST00000346085.10:c.4998C>G	ENSP00000344546.5:p.Val1666=
ENST00000350026.10:c.4710C>G	ENSP00000055163.7:p.Val1570=
ENST00000414678.7:c.3276C>G	ENSP00000412835.2:p.Val1092=
ENST00000635849.1:c.2439C>G	ENSP00000490948.1:p.Val813=
ENST00000635957.1:c.2070C>G	ENSP00000490385.1:p.Val690=
ENST00000636227.1:n.3581C>G
ENST00000636254.1:n.1038C>G
ENST00000636930.2:c.5118C>G MANE Select	ENSP00000490491.2:p.Val1706=
ENST00000636940.1:n.3115C>G
ENST00000637015.1:c.2486C>G
ENST00000637568.1:c.2400C>G
ENST00000637741.1:n.1784C>G
ENST00000637810.1:c.2460C>G	ENSP00000489636.1:p.Val820=
ENST00000637904.1:c.2619C>G	ENSP00000490550.1:p.Val873=
ENST00000647938.1:c.4749C>G	ENSP00000498155.1:p.Val1583=
ENST00000346085.9:c.4749C>G	ENSP00000344546.4:p.Val1583=
ENST00000350026.9:c.4710C>G	ENSP00000055163.7:p.Val1570=
ENST00000414678.6:c.3276C>G	ENSP00000412835.2:p.Val1092=
NM_017519.2:c.4710C>G	NP_059989.2:p.Val1570=
NM_020732.3:c.4749C>G	NP_065783.3:p.Val1583=
XM_005267069.3:c.4869C>G	XP_005267126.2:p.Val1623=
XM_011535984.1:c.3948C>G	XP_011534286.1:p.Val1316=
XM_011535985.1:c.3768C>G	XP_011534287.1:p.Val1256=
XM_011535986.1:c.3528C>G	XP_011534288.1:p.Val1176=
XM_011535987.1:c.3147C>G	XP_011534289.1:p.Val1049=
XM_011535988.1:c.2010C>G	XP_011534290.1:p.Val670=
NM_001346813.1:c.4869C>G	NP_001333742.1:p.Val1623=
NM_001363725.1:c.2619C>G	NP_001350654.1:p.Val873=
XM_011535984.2:c.5079C>G	XP_011534286.2:p.Val1693=
XM_011535988.3:c.2010C>G	XP_011534290.1:p.Val670=
XM_017011103.2:c.4980C>G	XP_016866592.1:p.Val1660=
XM_017011104.1:c.4950C>G	XP_016866593.1:p.Val1650=
XM_017011105.2:c.4920C>G	XP_016866594.1:p.Val1640=
XM_017011106.2:c.4791C>G	XP_016866595.1:p.Val1597=
XM_017011107.2:c.4770C>G	XP_016866596.1:p.Val1590=
XR_002956289.1:n.5065C>G
NM_001363725.2:c.2619C>G	NP_001350654.1:p.Val873=
NM_001371656.1:c.4998C>G	NP_001358585.1:p.Val1666=
NM_001374820.1:c.4998C>G	NP_001361749.1:p.Val1666=
NM_001374828.1:c.5118C>G MANE Select	NP_001361757.1:p.Val1706=
NM_017519.3:c.4959C>G	NP_059989.3:p.Val1653=