Canonical Allele Identifier: CA366242386

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522409C>A (hg19) ; chr6:g.157201275C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201275C>A , CM000668.2:g.157201275C>A	GRCh38
NC_000006.11:g.157522409C>A , CM000668.1:g.157522409C>A	GRCh37
NC_000006.10:g.157564101C>A	NCBI36
NG_032093.1:g.428346C>A
NG_032093.2:g.428346C>A
NG_066624.1:g.430250C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4891C>A	ENSP00000055163.8:p.Arg1631Ser
ENST00000414678.8:c.4960C>A	ENSP00000412835.3:p.Arg1654Ser
ENST00000637015.2:c.5179C>A	ENSP00000489729.2:p.Arg1727Ser
ENST00000346085.10:c.4930C>A	ENSP00000344546.5:p.Arg1644Ser
ENST00000350026.10:c.4642C>A	ENSP00000055163.7:p.Arg1548Ser
ENST00000414678.7:c.3208C>A	ENSP00000412835.2:p.Arg1070Ser
ENST00000635849.1:c.2371C>A	ENSP00000490948.1:p.Arg791Ser
ENST00000635957.1:c.2002C>A	ENSP00000490385.1:p.Arg668Ser
ENST00000636227.1:n.3513C>A
ENST00000636254.1:n.970C>A
ENST00000636930.2:c.5050C>A MANE Select	ENSP00000490491.2:p.Arg1684Ser
ENST00000636940.1:n.3047C>A
ENST00000637015.1:c.2418C>A
ENST00000637568.1:c.2332C>A
ENST00000637741.1:n.1716C>A
ENST00000637810.1:c.2392C>A	ENSP00000489636.1:p.Arg798Ser
ENST00000637904.1:c.2551C>A	ENSP00000490550.1:p.Arg851Ser
ENST00000647938.1:c.4681C>A	ENSP00000498155.1:p.Arg1561Ser
ENST00000346085.9:c.4681C>A	ENSP00000344546.4:p.Arg1561Ser
ENST00000350026.9:c.4642C>A	ENSP00000055163.7:p.Arg1548Ser
ENST00000414678.6:c.3208C>A	ENSP00000412835.2:p.Arg1070Ser
NM_017519.2:c.4642C>A	NP_059989.2:p.Arg1548Ser
NM_020732.3:c.4681C>A	NP_065783.3:p.Arg1561Ser
XM_005267069.3:c.4801C>A	XP_005267126.2:p.Arg1601Ser
XM_011535984.1:c.3880C>A	XP_011534286.1:p.Arg1294Ser
XM_011535985.1:c.3700C>A	XP_011534287.1:p.Arg1234Ser
XM_011535986.1:c.3460C>A	XP_011534288.1:p.Arg1154Ser
XM_011535987.1:c.3079C>A	XP_011534289.1:p.Arg1027Ser
XM_011535988.1:c.1942C>A	XP_011534290.1:p.Arg648Ser
NM_001346813.1:c.4801C>A	NP_001333742.1:p.Arg1601Ser
NM_001363725.1:c.2551C>A	NP_001350654.1:p.Arg851Ser
XM_011535984.2:c.5011C>A	XP_011534286.2:p.Arg1671Ser
XM_011535988.3:c.1942C>A	XP_011534290.1:p.Arg648Ser
XM_017011103.2:c.4912C>A	XP_016866592.1:p.Arg1638Ser
XM_017011104.1:c.4882C>A	XP_016866593.1:p.Arg1628Ser
XM_017011105.2:c.4852C>A	XP_016866594.1:p.Arg1618Ser
XM_017011106.2:c.4723C>A	XP_016866595.1:p.Arg1575Ser
XM_017011107.2:c.4702C>A	XP_016866596.1:p.Arg1568Ser
XR_002956289.1:n.4997C>A
NM_001363725.2:c.2551C>A	NP_001350654.1:p.Arg851Ser
NM_001371656.1:c.4930C>A	NP_001358585.1:p.Arg1644Ser
NM_001374820.1:c.4930C>A	NP_001361749.1:p.Arg1644Ser
NM_001374828.1:c.5050C>A MANE Select	NP_001361757.1:p.Arg1684Ser
NM_017519.3:c.4891C>A	NP_059989.3:p.Arg1631Ser