Canonical Allele Identifier: CA150370441

Gene: ARID1B

Linked Data

• dbSNP Id: rs910598795
• gnomAD v3: 6-157201372-C-G
• gnomAD v4: 6-157201372-C-G
• MyVariant Identifiers: chr6:g.157522506C>G (hg19) ; chr6:g.157201372C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201372C>G , CM000668.2:g.157201372C>G	GRCh38
NC_000006.11:g.157522506C>G , CM000668.1:g.157522506C>G	GRCh37
NC_000006.10:g.157564198C>G	NCBI36
NG_032093.1:g.428443C>G
NG_032093.2:g.428443C>G
NG_066624.1:g.430347C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4988C>G	ENSP00000055163.8:p.Thr1663Ser
ENST00000414678.8:c.5057C>G	ENSP00000412835.3:p.Thr1686Ser
ENST00000637015.2:c.5276C>G	ENSP00000489729.2:p.Thr1759Ser
ENST00000346085.10:c.5027C>G	ENSP00000344546.5:p.Thr1676Ser
ENST00000350026.10:c.4739C>G	ENSP00000055163.7:p.Thr1580Ser
ENST00000414678.7:c.3305C>G	ENSP00000412835.2:p.Thr1102Ser
ENST00000635849.1:c.2468C>G	ENSP00000490948.1:p.Thr823Ser
ENST00000635957.1:c.2099C>G	ENSP00000490385.1:p.Thr700Ser
ENST00000636227.1:n.3610C>G
ENST00000636254.1:n.1067C>G
ENST00000636930.2:c.5147C>G MANE Select	ENSP00000490491.2:p.Thr1716Ser
ENST00000636940.1:n.3144C>G
ENST00000637015.1:c.2515C>G
ENST00000637568.1:c.2429C>G
ENST00000637741.1:n.1813C>G
ENST00000637810.1:c.2489C>G	ENSP00000489636.1:p.Thr830Ser
ENST00000637904.1:c.2648C>G	ENSP00000490550.1:p.Thr883Ser
ENST00000647938.1:c.4778C>G	ENSP00000498155.1:p.Thr1593Ser
ENST00000346085.9:c.4778C>G	ENSP00000344546.4:p.Thr1593Ser
ENST00000350026.9:c.4739C>G	ENSP00000055163.7:p.Thr1580Ser
ENST00000414678.6:c.3305C>G	ENSP00000412835.2:p.Thr1102Ser
NM_017519.2:c.4739C>G	NP_059989.2:p.Thr1580Ser
NM_020732.3:c.4778C>G	NP_065783.3:p.Thr1593Ser
XM_005267069.3:c.4898C>G	XP_005267126.2:p.Thr1633Ser
XM_011535984.1:c.3977C>G	XP_011534286.1:p.Thr1326Ser
XM_011535985.1:c.3797C>G	XP_011534287.1:p.Thr1266Ser
XM_011535986.1:c.3557C>G	XP_011534288.1:p.Thr1186Ser
XM_011535987.1:c.3176C>G	XP_011534289.1:p.Thr1059Ser
XM_011535988.1:c.2039C>G	XP_011534290.1:p.Thr680Ser
NM_001346813.1:c.4898C>G	NP_001333742.1:p.Thr1633Ser
NM_001363725.1:c.2648C>G	NP_001350654.1:p.Thr883Ser
XM_011535984.2:c.5108C>G	XP_011534286.2:p.Thr1703Ser
XM_011535988.3:c.2039C>G	XP_011534290.1:p.Thr680Ser
XM_017011103.2:c.5009C>G	XP_016866592.1:p.Thr1670Ser
XM_017011104.1:c.4979C>G	XP_016866593.1:p.Thr1660Ser
XM_017011105.2:c.4949C>G	XP_016866594.1:p.Thr1650Ser
XM_017011106.2:c.4820C>G	XP_016866595.1:p.Thr1607Ser
XM_017011107.2:c.4799C>G	XP_016866596.1:p.Thr1600Ser
XR_002956289.1:n.5094C>G
NM_001363725.2:c.2648C>G	NP_001350654.1:p.Thr883Ser
NM_001371656.1:c.5027C>G	NP_001358585.1:p.Thr1676Ser
NM_001374820.1:c.5027C>G	NP_001361749.1:p.Thr1676Ser
NM_001374828.1:c.5147C>G MANE Select	NP_001361757.1:p.Thr1716Ser
NM_017519.3:c.4988C>G	NP_059989.3:p.Thr1663Ser