Canonical Allele Identifier: CA366242445

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375796
• MyVariant Identifiers: chr6:g.157522438C>A (hg19) ; chr6:g.157201304C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201304C>A , CM000668.2:g.157201304C>A	GRCh38
NC_000006.11:g.157522438C>A , CM000668.1:g.157522438C>A	GRCh37
NC_000006.10:g.157564130C>A	NCBI36
NG_032093.1:g.428375C>A
NG_032093.2:g.428375C>A
NG_066624.1:g.430279C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4920C>A	ENSP00000055163.8:p.Ser1640Arg
ENST00000414678.8:c.4989C>A	ENSP00000412835.3:p.Ser1663Arg
ENST00000637015.2:c.5208C>A	ENSP00000489729.2:p.Ser1736Arg
ENST00000346085.10:c.4959C>A	ENSP00000344546.5:p.Ser1653Arg
ENST00000350026.10:c.4671C>A	ENSP00000055163.7:p.Ser1557Arg
ENST00000414678.7:c.3237C>A	ENSP00000412835.2:p.Ser1079Arg
ENST00000635849.1:c.2400C>A	ENSP00000490948.1:p.Ser800Arg
ENST00000635957.1:c.2031C>A	ENSP00000490385.1:p.Ser677Arg
ENST00000636227.1:n.3542C>A
ENST00000636254.1:n.999C>A
ENST00000636930.2:c.5079C>A MANE Select	ENSP00000490491.2:p.Ser1693Arg
ENST00000636940.1:n.3076C>A
ENST00000637015.1:c.2447C>A
ENST00000637568.1:c.2361C>A
ENST00000637741.1:n.1745C>A
ENST00000637810.1:c.2421C>A	ENSP00000489636.1:p.Ser807Arg
ENST00000637904.1:c.2580C>A	ENSP00000490550.1:p.Ser860Arg
ENST00000647938.1:c.4710C>A	ENSP00000498155.1:p.Ser1570Arg
ENST00000346085.9:c.4710C>A	ENSP00000344546.4:p.Ser1570Arg
ENST00000350026.9:c.4671C>A	ENSP00000055163.7:p.Ser1557Arg
ENST00000414678.6:c.3237C>A	ENSP00000412835.2:p.Ser1079Arg
NM_017519.2:c.4671C>A	NP_059989.2:p.Ser1557Arg
NM_020732.3:c.4710C>A	NP_065783.3:p.Ser1570Arg
XM_005267069.3:c.4830C>A	XP_005267126.2:p.Ser1610Arg
XM_011535984.1:c.3909C>A	XP_011534286.1:p.Ser1303Arg
XM_011535985.1:c.3729C>A	XP_011534287.1:p.Ser1243Arg
XM_011535986.1:c.3489C>A	XP_011534288.1:p.Ser1163Arg
XM_011535987.1:c.3108C>A	XP_011534289.1:p.Ser1036Arg
XM_011535988.1:c.1971C>A	XP_011534290.1:p.Ser657Arg
NM_001346813.1:c.4830C>A	NP_001333742.1:p.Ser1610Arg
NM_001363725.1:c.2580C>A	NP_001350654.1:p.Ser860Arg
XM_011535984.2:c.5040C>A	XP_011534286.2:p.Ser1680Arg
XM_011535988.3:c.1971C>A	XP_011534290.1:p.Ser657Arg
XM_017011103.2:c.4941C>A	XP_016866592.1:p.Ser1647Arg
XM_017011104.1:c.4911C>A	XP_016866593.1:p.Ser1637Arg
XM_017011105.2:c.4881C>A	XP_016866594.1:p.Ser1627Arg
XM_017011106.2:c.4752C>A	XP_016866595.1:p.Ser1584Arg
XM_017011107.2:c.4731C>A	XP_016866596.1:p.Ser1577Arg
XR_002956289.1:n.5026C>A
NM_001363725.2:c.2580C>A	NP_001350654.1:p.Ser860Arg
NM_001371656.1:c.4959C>A	NP_001358585.1:p.Ser1653Arg
NM_001374820.1:c.4959C>A	NP_001361749.1:p.Ser1653Arg
NM_001374828.1:c.5079C>A MANE Select	NP_001361757.1:p.Ser1693Arg
NM_017519.3:c.4920C>A	NP_059989.3:p.Ser1640Arg