Canonical Allele Identifier: CA452978177

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375253
• MyVariant Identifiers: chr6:g.157522345C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201211C>A , CM000668.2:g.157201211C>A	GRCh38
NC_000006.11:g.157522345C>A , CM000668.1:g.157522345C>A	GRCh37
NC_000006.10:g.157564037C>A	NCBI36
NG_032093.1:g.428282C>A
NG_032093.2:g.428282C>A
NG_066624.1:g.430186C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4827C>A	ENSP00000055163.8:p.Ser1609=
ENST00000414678.8:c.4896C>A	ENSP00000412835.3:p.Ser1632=
ENST00000637015.2:c.5115C>A	ENSP00000489729.2:p.Ser1705=
ENST00000346085.10:c.4866C>A	ENSP00000344546.5:p.Ser1622=
ENST00000350026.10:c.4578C>A	ENSP00000055163.7:p.Ser1526=
ENST00000414678.7:c.3144C>A	ENSP00000412835.2:p.Ser1048=
ENST00000635849.1:c.2307C>A	ENSP00000490948.1:p.Ser769=
ENST00000635957.1:c.1938C>A	ENSP00000490385.1:p.Ser646=
ENST00000636227.1:n.3449C>A
ENST00000636254.1:n.906C>A
ENST00000636930.2:c.4986C>A MANE Select	ENSP00000490491.2:p.Ser1662=
ENST00000636940.1:n.2983C>A
ENST00000637015.1:c.2354C>A
ENST00000637568.1:c.2268C>A
ENST00000637741.1:n.1652C>A
ENST00000637810.1:c.2328C>A	ENSP00000489636.1:p.Ser776=
ENST00000637904.1:c.2487C>A	ENSP00000490550.1:p.Ser829=
ENST00000647938.1:c.4617C>A	ENSP00000498155.1:p.Ser1539=
ENST00000346085.9:c.4617C>A	ENSP00000344546.4:p.Ser1539=
ENST00000350026.9:c.4578C>A	ENSP00000055163.7:p.Ser1526=
ENST00000414678.6:c.3144C>A	ENSP00000412835.2:p.Ser1048=
NM_017519.2:c.4578C>A	NP_059989.2:p.Ser1526=
NM_020732.3:c.4617C>A	NP_065783.3:p.Ser1539=
XM_005267069.3:c.4737C>A	XP_005267126.2:p.Ser1579=
XM_011535984.1:c.3816C>A	XP_011534286.1:p.Ser1272=
XM_011535985.1:c.3636C>A	XP_011534287.1:p.Ser1212=
XM_011535986.1:c.3396C>A	XP_011534288.1:p.Ser1132=
XM_011535987.1:c.3015C>A	XP_011534289.1:p.Ser1005=
XM_011535988.1:c.1878C>A	XP_011534290.1:p.Ser626=
NM_001346813.1:c.4737C>A	NP_001333742.1:p.Ser1579=
NM_001363725.1:c.2487C>A	NP_001350654.1:p.Ser829=
XM_011535984.2:c.4947C>A	XP_011534286.2:p.Ser1649=
XM_011535988.3:c.1878C>A	XP_011534290.1:p.Ser626=
XM_017011103.2:c.4848C>A	XP_016866592.1:p.Ser1616=
XM_017011104.1:c.4818C>A	XP_016866593.1:p.Ser1606=
XM_017011105.2:c.4788C>A	XP_016866594.1:p.Ser1596=
XM_017011106.2:c.4659C>A	XP_016866595.1:p.Ser1553=
XM_017011107.2:c.4638C>A	XP_016866596.1:p.Ser1546=
XR_002956289.1:n.4933C>A
NM_001363725.2:c.2487C>A	NP_001350654.1:p.Ser829=
NM_001371656.1:c.4866C>A	NP_001358585.1:p.Ser1622=
NM_001374820.1:c.4866C>A	NP_001361749.1:p.Ser1622=
NM_001374828.1:c.4986C>A MANE Select	NP_001361757.1:p.Ser1662=
NM_017519.3:c.4827C>A	NP_059989.3:p.Ser1609=