Canonical Allele Identifier: CA452978162

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522330C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201196C>G , CM000668.2:g.157201196C>G	GRCh38
NC_000006.11:g.157522330C>G , CM000668.1:g.157522330C>G	GRCh37
NC_000006.10:g.157564022C>G	NCBI36
NG_032093.1:g.428267C>G
NG_032093.2:g.428267C>G
NG_066624.1:g.430171C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4812C>G	ENSP00000055163.8:p.Arg1604=
ENST00000414678.8:c.4881C>G	ENSP00000412835.3:p.Arg1627=
ENST00000637015.2:c.5100C>G	ENSP00000489729.2:p.Arg1700=
ENST00000346085.10:c.4851C>G	ENSP00000344546.5:p.Arg1617=
ENST00000350026.10:c.4563C>G	ENSP00000055163.7:p.Arg1521=
ENST00000414678.7:c.3129C>G	ENSP00000412835.2:p.Arg1043=
ENST00000635849.1:c.2292C>G	ENSP00000490948.1:p.Arg764=
ENST00000635957.1:c.1923C>G	ENSP00000490385.1:p.Arg641=
ENST00000636227.1:n.3434C>G
ENST00000636254.1:n.891C>G
ENST00000636930.2:c.4971C>G MANE Select	ENSP00000490491.2:p.Arg1657=
ENST00000636940.1:n.2968C>G
ENST00000637015.1:c.2339C>G
ENST00000637568.1:c.2253C>G
ENST00000637741.1:n.1637C>G
ENST00000637810.1:c.2313C>G	ENSP00000489636.1:p.Arg771=
ENST00000637904.1:c.2472C>G	ENSP00000490550.1:p.Arg824=
ENST00000647938.1:c.4602C>G	ENSP00000498155.1:p.Arg1534=
ENST00000346085.9:c.4602C>G	ENSP00000344546.4:p.Arg1534=
ENST00000350026.9:c.4563C>G	ENSP00000055163.7:p.Arg1521=
ENST00000414678.6:c.3129C>G	ENSP00000412835.2:p.Arg1043=
NM_017519.2:c.4563C>G	NP_059989.2:p.Arg1521=
NM_020732.3:c.4602C>G	NP_065783.3:p.Arg1534=
XM_005267069.3:c.4722C>G	XP_005267126.2:p.Arg1574=
XM_011535984.1:c.3801C>G	XP_011534286.1:p.Arg1267=
XM_011535985.1:c.3621C>G	XP_011534287.1:p.Arg1207=
XM_011535986.1:c.3381C>G	XP_011534288.1:p.Arg1127=
XM_011535987.1:c.3000C>G	XP_011534289.1:p.Arg1000=
XM_011535988.1:c.1863C>G	XP_011534290.1:p.Arg621=
NM_001346813.1:c.4722C>G	NP_001333742.1:p.Arg1574=
NM_001363725.1:c.2472C>G	NP_001350654.1:p.Arg824=
XM_011535984.2:c.4932C>G	XP_011534286.2:p.Arg1644=
XM_011535988.3:c.1863C>G	XP_011534290.1:p.Arg621=
XM_017011103.2:c.4833C>G	XP_016866592.1:p.Arg1611=
XM_017011104.1:c.4803C>G	XP_016866593.1:p.Arg1601=
XM_017011105.2:c.4773C>G	XP_016866594.1:p.Arg1591=
XM_017011106.2:c.4644C>G	XP_016866595.1:p.Arg1548=
XM_017011107.2:c.4623C>G	XP_016866596.1:p.Arg1541=
XR_002956289.1:n.4918C>G
NM_001363725.2:c.2472C>G	NP_001350654.1:p.Arg824=
NM_001371656.1:c.4851C>G	NP_001358585.1:p.Arg1617=
NM_001374820.1:c.4851C>G	NP_001361749.1:p.Arg1617=
NM_001374828.1:c.4971C>G MANE Select	NP_001361757.1:p.Arg1657=
NM_017519.3:c.4812C>G	NP_059989.3:p.Arg1604=