Canonical Allele Identifier: CA452978376

Gene: ARID1B

Linked Data

• dbSNP Id: rs139903653
• MyVariant Identifiers: chr6:g.157522168C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201034C>G , CM000668.2:g.157201034C>G	GRCh38
NC_000006.11:g.157522168C>G , CM000668.1:g.157522168C>G	GRCh37
NC_000006.10:g.157563860C>G	NCBI36
NG_032093.1:g.428105C>G
NG_032093.2:g.428105C>G
NG_066624.1:g.430009C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4650C>G	ENSP00000055163.8:p.Gly1550=
ENST00000414678.8:c.4719C>G	ENSP00000412835.3:p.Gly1573=
ENST00000637015.2:c.4938C>G	ENSP00000489729.2:p.Gly1646=
ENST00000346085.10:c.4689C>G	ENSP00000344546.5:p.Gly1563=
ENST00000350026.10:c.4401C>G	ENSP00000055163.7:p.Gly1467=
ENST00000414678.7:c.2967C>G	ENSP00000412835.2:p.Gly989=
ENST00000635849.1:c.2130C>G	ENSP00000490948.1:p.Gly710=
ENST00000635957.1:c.1761C>G	ENSP00000490385.1:p.Gly587=
ENST00000636227.1:n.3272C>G
ENST00000636254.1:n.729C>G
ENST00000636930.2:c.4809C>G MANE Select	ENSP00000490491.2:p.Gly1603=
ENST00000636940.1:n.2806C>G
ENST00000637015.1:c.2177C>G
ENST00000637568.1:c.2091C>G
ENST00000637741.1:n.1475C>G
ENST00000637810.1:c.2151C>G	ENSP00000489636.1:p.Gly717=
ENST00000637904.1:c.2310C>G	ENSP00000490550.1:p.Gly770=
ENST00000647938.1:c.4440C>G	ENSP00000498155.1:p.Gly1480=
ENST00000346085.9:c.4440C>G	ENSP00000344546.4:p.Gly1480=
ENST00000350026.9:c.4401C>G	ENSP00000055163.7:p.Gly1467=
ENST00000414678.6:c.2967C>G	ENSP00000412835.2:p.Gly989=
NM_017519.2:c.4401C>G	NP_059989.2:p.Gly1467=
NM_020732.3:c.4440C>G	NP_065783.3:p.Gly1480=
XM_005267069.3:c.4560C>G	XP_005267126.2:p.Gly1520=
XM_011535984.1:c.3639C>G	XP_011534286.1:p.Gly1213=
XM_011535985.1:c.3459C>G	XP_011534287.1:p.Gly1153=
XM_011535986.1:c.3219C>G	XP_011534288.1:p.Gly1073=
XM_011535987.1:c.2838C>G	XP_011534289.1:p.Gly946=
XM_011535988.1:c.1701C>G	XP_011534290.1:p.Gly567=
NM_001346813.1:c.4560C>G	NP_001333742.1:p.Gly1520=
NM_001363725.1:c.2310C>G	NP_001350654.1:p.Gly770=
XM_011535984.2:c.4770C>G	XP_011534286.2:p.Gly1590=
XM_011535988.3:c.1701C>G	XP_011534290.1:p.Gly567=
XM_017011103.2:c.4671C>G	XP_016866592.1:p.Gly1557=
XM_017011104.1:c.4641C>G	XP_016866593.1:p.Gly1547=
XM_017011105.2:c.4611C>G	XP_016866594.1:p.Gly1537=
XM_017011106.2:c.4482C>G	XP_016866595.1:p.Gly1494=
XM_017011107.2:c.4461C>G	XP_016866596.1:p.Gly1487=
XR_002956289.1:n.4756C>G
NM_001363725.2:c.2310C>G	NP_001350654.1:p.Gly770=
NM_001371656.1:c.4689C>G	NP_001358585.1:p.Gly1563=
NM_001374820.1:c.4689C>G	NP_001361749.1:p.Gly1563=
NM_001374828.1:c.4809C>G MANE Select	NP_001361757.1:p.Gly1603=
NM_017519.3:c.4650C>G	NP_059989.3:p.Gly1550=