Canonical Allele Identifier: CA366241389

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522125C>G (hg19) ; chr6:g.157200991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200991C>G , CM000668.2:g.157200991C>G	GRCh38
NC_000006.11:g.157522125C>G , CM000668.1:g.157522125C>G	GRCh37
NC_000006.10:g.157563817C>G	NCBI36
NG_032093.1:g.428062C>G
NG_032093.2:g.428062C>G
NG_066624.1:g.429966C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4607C>G	ENSP00000055163.8:p.Ala1536Gly
ENST00000414678.8:c.4676C>G	ENSP00000412835.3:p.Ala1559Gly
ENST00000637015.2:c.4895C>G	ENSP00000489729.2:p.Ala1632Gly
ENST00000346085.10:c.4646C>G	ENSP00000344546.5:p.Ala1549Gly
ENST00000350026.10:c.4358C>G	ENSP00000055163.7:p.Ala1453Gly
ENST00000414678.7:c.2924C>G	ENSP00000412835.2:p.Ala975Gly
ENST00000635849.1:c.2087C>G	ENSP00000490948.1:p.Ala696Gly
ENST00000635957.1:c.1718C>G	ENSP00000490385.1:p.Ala573Gly
ENST00000636227.1:n.3229C>G
ENST00000636254.1:n.686C>G
ENST00000636930.2:c.4766C>G MANE Select	ENSP00000490491.2:p.Ala1589Gly
ENST00000636940.1:n.2763C>G
ENST00000637015.1:c.2134C>G
ENST00000637568.1:c.2048C>G
ENST00000637741.1:n.1432C>G
ENST00000637810.1:c.2108C>G	ENSP00000489636.1:p.Ala703Gly
ENST00000637904.1:c.2267C>G	ENSP00000490550.1:p.Ala756Gly
ENST00000647938.1:c.4397C>G	ENSP00000498155.1:p.Ala1466Gly
ENST00000346085.9:c.4397C>G	ENSP00000344546.4:p.Ala1466Gly
ENST00000350026.9:c.4358C>G	ENSP00000055163.7:p.Ala1453Gly
ENST00000414678.6:c.2924C>G	ENSP00000412835.2:p.Ala975Gly
NM_017519.2:c.4358C>G	NP_059989.2:p.Ala1453Gly
NM_020732.3:c.4397C>G	NP_065783.3:p.Ala1466Gly
XM_005267069.3:c.4517C>G	XP_005267126.2:p.Ala1506Gly
XM_011535984.1:c.3596C>G	XP_011534286.1:p.Ala1199Gly
XM_011535985.1:c.3416C>G	XP_011534287.1:p.Ala1139Gly
XM_011535986.1:c.3176C>G	XP_011534288.1:p.Ala1059Gly
XM_011535987.1:c.2795C>G	XP_011534289.1:p.Ala932Gly
XM_011535988.1:c.1658C>G	XP_011534290.1:p.Ala553Gly
NM_001346813.1:c.4517C>G	NP_001333742.1:p.Ala1506Gly
NM_001363725.1:c.2267C>G	NP_001350654.1:p.Ala756Gly
XM_011535984.2:c.4727C>G	XP_011534286.2:p.Ala1576Gly
XM_011535988.3:c.1658C>G	XP_011534290.1:p.Ala553Gly
XM_017011103.2:c.4628C>G	XP_016866592.1:p.Ala1543Gly
XM_017011104.1:c.4598C>G	XP_016866593.1:p.Ala1533Gly
XM_017011105.2:c.4568C>G	XP_016866594.1:p.Ala1523Gly
XM_017011106.2:c.4439C>G	XP_016866595.1:p.Ala1480Gly
XM_017011107.2:c.4418C>G	XP_016866596.1:p.Ala1473Gly
XR_002956289.1:n.4713C>G
NM_001363725.2:c.2267C>G	NP_001350654.1:p.Ala756Gly
NM_001371656.1:c.4646C>G	NP_001358585.1:p.Ala1549Gly
NM_001374820.1:c.4646C>G	NP_001361749.1:p.Ala1549Gly
NM_001374828.1:c.4766C>G MANE Select	NP_001361757.1:p.Ala1589Gly
NM_017519.3:c.4607C>G	NP_059989.3:p.Ala1536Gly