Canonical Allele Identifier: CA452978265

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522411C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201277C>A , CM000668.2:g.157201277C>A	GRCh38
NC_000006.11:g.157522411C>A , CM000668.1:g.157522411C>A	GRCh37
NC_000006.10:g.157564103C>A	NCBI36
NG_032093.1:g.428348C>A
NG_032093.2:g.428348C>A
NG_066624.1:g.430252C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4893C>A	ENSP00000055163.8:p.Arg1631=
ENST00000414678.8:c.4962C>A	ENSP00000412835.3:p.Arg1654=
ENST00000637015.2:c.5181C>A	ENSP00000489729.2:p.Arg1727=
ENST00000346085.10:c.4932C>A	ENSP00000344546.5:p.Arg1644=
ENST00000350026.10:c.4644C>A	ENSP00000055163.7:p.Arg1548=
ENST00000414678.7:c.3210C>A	ENSP00000412835.2:p.Arg1070=
ENST00000635849.1:c.2373C>A	ENSP00000490948.1:p.Arg791=
ENST00000635957.1:c.2004C>A	ENSP00000490385.1:p.Arg668=
ENST00000636227.1:n.3515C>A
ENST00000636254.1:n.972C>A
ENST00000636930.2:c.5052C>A MANE Select	ENSP00000490491.2:p.Arg1684=
ENST00000636940.1:n.3049C>A
ENST00000637015.1:c.2420C>A
ENST00000637568.1:c.2334C>A
ENST00000637741.1:n.1718C>A
ENST00000637810.1:c.2394C>A	ENSP00000489636.1:p.Arg798=
ENST00000637904.1:c.2553C>A	ENSP00000490550.1:p.Arg851=
ENST00000647938.1:c.4683C>A	ENSP00000498155.1:p.Arg1561=
ENST00000346085.9:c.4683C>A	ENSP00000344546.4:p.Arg1561=
ENST00000350026.9:c.4644C>A	ENSP00000055163.7:p.Arg1548=
ENST00000414678.6:c.3210C>A	ENSP00000412835.2:p.Arg1070=
NM_017519.2:c.4644C>A	NP_059989.2:p.Arg1548=
NM_020732.3:c.4683C>A	NP_065783.3:p.Arg1561=
XM_005267069.3:c.4803C>A	XP_005267126.2:p.Arg1601=
XM_011535984.1:c.3882C>A	XP_011534286.1:p.Arg1294=
XM_011535985.1:c.3702C>A	XP_011534287.1:p.Arg1234=
XM_011535986.1:c.3462C>A	XP_011534288.1:p.Arg1154=
XM_011535987.1:c.3081C>A	XP_011534289.1:p.Arg1027=
XM_011535988.1:c.1944C>A	XP_011534290.1:p.Arg648=
NM_001346813.1:c.4803C>A	NP_001333742.1:p.Arg1601=
NM_001363725.1:c.2553C>A	NP_001350654.1:p.Arg851=
XM_011535984.2:c.5013C>A	XP_011534286.2:p.Arg1671=
XM_011535988.3:c.1944C>A	XP_011534290.1:p.Arg648=
XM_017011103.2:c.4914C>A	XP_016866592.1:p.Arg1638=
XM_017011104.1:c.4884C>A	XP_016866593.1:p.Arg1628=
XM_017011105.2:c.4854C>A	XP_016866594.1:p.Arg1618=
XM_017011106.2:c.4725C>A	XP_016866595.1:p.Arg1575=
XM_017011107.2:c.4704C>A	XP_016866596.1:p.Arg1568=
XR_002956289.1:n.4999C>A
NM_001363725.2:c.2553C>A	NP_001350654.1:p.Arg851=
NM_001371656.1:c.4932C>A	NP_001358585.1:p.Arg1644=
NM_001374820.1:c.4932C>A	NP_001361749.1:p.Arg1644=
NM_001374828.1:c.5052C>A MANE Select	NP_001361757.1:p.Arg1684=
NM_017519.3:c.4893C>A	NP_059989.3:p.Arg1631=