Canonical Allele Identifier: CA452784853

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522538A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201404A>C , CM000668.2:g.157201404A>C	GRCh38
NC_000006.11:g.157522538A>C , CM000668.1:g.157522538A>C	GRCh37
NC_000006.10:g.157564230A>C	NCBI36
NG_032093.1:g.428475A>C
NG_032093.2:g.428475A>C
NG_066624.1:g.430379A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5020A>C	ENSP00000055163.8:p.Arg1674=
ENST00000414678.8:c.5089A>C	ENSP00000412835.3:p.Arg1697=
ENST00000637015.2:c.5308A>C	ENSP00000489729.2:p.Arg1770=
ENST00000346085.10:c.5059A>C	ENSP00000344546.5:p.Arg1687=
ENST00000350026.10:c.4771A>C	ENSP00000055163.7:p.Arg1591=
ENST00000414678.7:c.3337A>C	ENSP00000412835.2:p.Arg1113=
ENST00000635849.1:c.2500A>C	ENSP00000490948.1:p.Arg834=
ENST00000635957.1:c.2131A>C	ENSP00000490385.1:p.Arg711=
ENST00000636227.1:n.3642A>C
ENST00000636254.1:n.1099A>C
ENST00000636930.2:c.5179A>C MANE Select	ENSP00000490491.2:p.Arg1727=
ENST00000636940.1:n.3176A>C
ENST00000637015.1:c.2547A>C
ENST00000637568.1:c.2461A>C
ENST00000637741.1:n.1845A>C
ENST00000637810.1:c.2521A>C	ENSP00000489636.1:p.Arg841=
ENST00000637904.1:c.2680A>C	ENSP00000490550.1:p.Arg894=
ENST00000647938.1:c.4810A>C	ENSP00000498155.1:p.Arg1604=
ENST00000346085.9:c.4810A>C	ENSP00000344546.4:p.Arg1604=
ENST00000350026.9:c.4771A>C	ENSP00000055163.7:p.Arg1591=
ENST00000414678.6:c.3337A>C	ENSP00000412835.2:p.Arg1113=
NM_017519.2:c.4771A>C	NP_059989.2:p.Arg1591=
NM_020732.3:c.4810A>C	NP_065783.3:p.Arg1604=
XM_005267069.3:c.4930A>C	XP_005267126.2:p.Arg1644=
XM_011535984.1:c.4009A>C	XP_011534286.1:p.Arg1337=
XM_011535985.1:c.3829A>C	XP_011534287.1:p.Arg1277=
XM_011535986.1:c.3589A>C	XP_011534288.1:p.Arg1197=
XM_011535987.1:c.3208A>C	XP_011534289.1:p.Arg1070=
XM_011535988.1:c.2071A>C	XP_011534290.1:p.Arg691=
NM_001346813.1:c.4930A>C	NP_001333742.1:p.Arg1644=
NM_001363725.1:c.2680A>C	NP_001350654.1:p.Arg894=
XM_011535984.2:c.5140A>C	XP_011534286.2:p.Arg1714=
XM_011535988.3:c.2071A>C	XP_011534290.1:p.Arg691=
XM_017011103.2:c.5041A>C	XP_016866592.1:p.Arg1681=
XM_017011104.1:c.5011A>C	XP_016866593.1:p.Arg1671=
XM_017011105.2:c.4981A>C	XP_016866594.1:p.Arg1661=
XM_017011106.2:c.4852A>C	XP_016866595.1:p.Arg1618=
XM_017011107.2:c.4831A>C	XP_016866596.1:p.Arg1611=
XR_002956289.1:n.5126A>C
NM_001363725.2:c.2680A>C	NP_001350654.1:p.Arg894=
NM_001371656.1:c.5059A>C	NP_001358585.1:p.Arg1687=
NM_001374820.1:c.5059A>C	NP_001361749.1:p.Arg1687=
NM_001374828.1:c.5179A>C MANE Select	NP_001361757.1:p.Arg1727=
NM_017519.3:c.5020A>C	NP_059989.3:p.Arg1674=