Canonical Allele Identifier: CA452978320

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522132C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200998C>T , CM000668.2:g.157200998C>T	GRCh38
NC_000006.11:g.157522132C>T , CM000668.1:g.157522132C>T	GRCh37
NC_000006.10:g.157563824C>T	NCBI36
NG_032093.1:g.428069C>T
NG_032093.2:g.428069C>T
NG_066624.1:g.429973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4614C>T	ENSP00000055163.8:p.Arg1538=
ENST00000414678.8:c.4683C>T	ENSP00000412835.3:p.Arg1561=
ENST00000637015.2:c.4902C>T	ENSP00000489729.2:p.Arg1634=
ENST00000346085.10:c.4653C>T	ENSP00000344546.5:p.Arg1551=
ENST00000350026.10:c.4365C>T	ENSP00000055163.7:p.Arg1455=
ENST00000414678.7:c.2931C>T	ENSP00000412835.2:p.Arg977=
ENST00000635849.1:c.2094C>T	ENSP00000490948.1:p.Arg698=
ENST00000635957.1:c.1725C>T	ENSP00000490385.1:p.Arg575=
ENST00000636227.1:n.3236C>T
ENST00000636254.1:n.693C>T
ENST00000636930.2:c.4773C>T MANE Select	ENSP00000490491.2:p.Arg1591=
ENST00000636940.1:n.2770C>T
ENST00000637015.1:c.2141C>T
ENST00000637568.1:c.2055C>T
ENST00000637741.1:n.1439C>T
ENST00000637810.1:c.2115C>T	ENSP00000489636.1:p.Arg705=
ENST00000637904.1:c.2274C>T	ENSP00000490550.1:p.Arg758=
ENST00000647938.1:c.4404C>T	ENSP00000498155.1:p.Arg1468=
ENST00000346085.9:c.4404C>T	ENSP00000344546.4:p.Arg1468=
ENST00000350026.9:c.4365C>T	ENSP00000055163.7:p.Arg1455=
ENST00000414678.6:c.2931C>T	ENSP00000412835.2:p.Arg977=
NM_017519.2:c.4365C>T	NP_059989.2:p.Arg1455=
NM_020732.3:c.4404C>T	NP_065783.3:p.Arg1468=
XM_005267069.3:c.4524C>T	XP_005267126.2:p.Arg1508=
XM_011535984.1:c.3603C>T	XP_011534286.1:p.Arg1201=
XM_011535985.1:c.3423C>T	XP_011534287.1:p.Arg1141=
XM_011535986.1:c.3183C>T	XP_011534288.1:p.Arg1061=
XM_011535987.1:c.2802C>T	XP_011534289.1:p.Arg934=
XM_011535988.1:c.1665C>T	XP_011534290.1:p.Arg555=
NM_001346813.1:c.4524C>T	NP_001333742.1:p.Arg1508=
NM_001363725.1:c.2274C>T	NP_001350654.1:p.Arg758=
XM_011535984.2:c.4734C>T	XP_011534286.2:p.Arg1578=
XM_011535988.3:c.1665C>T	XP_011534290.1:p.Arg555=
XM_017011103.2:c.4635C>T	XP_016866592.1:p.Arg1545=
XM_017011104.1:c.4605C>T	XP_016866593.1:p.Arg1535=
XM_017011105.2:c.4575C>T	XP_016866594.1:p.Arg1525=
XM_017011106.2:c.4446C>T	XP_016866595.1:p.Arg1482=
XM_017011107.2:c.4425C>T	XP_016866596.1:p.Arg1475=
XR_002956289.1:n.4720C>T
NM_001363725.2:c.2274C>T	NP_001350654.1:p.Arg758=
NM_001371656.1:c.4653C>T	NP_001358585.1:p.Arg1551=
NM_001374820.1:c.4653C>T	NP_001361749.1:p.Arg1551=
NM_001374828.1:c.4773C>T MANE Select	NP_001361757.1:p.Arg1591=
NM_017519.3:c.4614C>T	NP_059989.3:p.Arg1538=