Canonical Allele Identifier: CA452977902

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2577973
• ClinVar RCV Id: RCV003325379
• dbSNP Id: rs1399194192
• MyVariant Identifiers: chr6:g.157522015G>A (hg19) ; chr6:g.157200881G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200881G>A , CM000668.2:g.157200881G>A	GRCh38
NC_000006.11:g.157522015G>A , CM000668.1:g.157522015G>A	GRCh37
NC_000006.10:g.157563707G>A	NCBI36
NG_032093.1:g.427952G>A
NG_032093.2:g.427952G>A
NG_066624.1:g.429856G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4497G>A	ENSP00000055163.8:p.Arg1499=
ENST00000414678.8:c.4566G>A	ENSP00000412835.3:p.Arg1522=
ENST00000637015.2:c.4785G>A	ENSP00000489729.2:p.Arg1595=
ENST00000346085.10:c.4536G>A	ENSP00000344546.5:p.Arg1512=
ENST00000350026.10:c.4248G>A	ENSP00000055163.7:p.Arg1416=
ENST00000414678.7:c.2814G>A	ENSP00000412835.2:p.Arg938=
ENST00000635849.1:c.1977G>A	ENSP00000490948.1:p.Arg659=
ENST00000635957.1:c.1608G>A	ENSP00000490385.1:p.Arg536=
ENST00000636227.1:n.3119G>A
ENST00000636254.1:n.576G>A
ENST00000636930.2:c.4656G>A MANE Select	ENSP00000490491.2:p.Arg1552=
ENST00000636940.1:n.2653G>A
ENST00000637015.1:c.2024G>A
ENST00000637568.1:c.1938G>A
ENST00000637741.1:n.1322G>A
ENST00000637810.1:c.1998G>A	ENSP00000489636.1:p.Arg666=
ENST00000637904.1:c.2157G>A	ENSP00000490550.1:p.Arg719=
ENST00000647938.1:c.4287G>A	ENSP00000498155.1:p.Arg1429=
ENST00000346085.9:c.4287G>A	ENSP00000344546.4:p.Arg1429=
ENST00000350026.9:c.4248G>A	ENSP00000055163.7:p.Arg1416=
ENST00000414678.6:c.2814G>A	ENSP00000412835.2:p.Arg938=
NM_017519.2:c.4248G>A	NP_059989.2:p.Arg1416=
NM_020732.3:c.4287G>A	NP_065783.3:p.Arg1429=
XM_005267069.3:c.4407G>A	XP_005267126.2:p.Arg1469=
XM_011535984.1:c.3486G>A	XP_011534286.1:p.Arg1162=
XM_011535985.1:c.3306G>A	XP_011534287.1:p.Arg1102=
XM_011535986.1:c.3066G>A	XP_011534288.1:p.Arg1022=
XM_011535987.1:c.2685G>A	XP_011534289.1:p.Arg895=
XM_011535988.1:c.1548G>A	XP_011534290.1:p.Arg516=
NM_001346813.1:c.4407G>A	NP_001333742.1:p.Arg1469=
NM_001363725.1:c.2157G>A	NP_001350654.1:p.Arg719=
XM_011535984.2:c.4617G>A	XP_011534286.2:p.Arg1539=
XM_011535988.3:c.1548G>A	XP_011534290.1:p.Arg516=
XM_017011103.2:c.4518G>A	XP_016866592.1:p.Arg1506=
XM_017011104.1:c.4488G>A	XP_016866593.1:p.Arg1496=
XM_017011105.2:c.4458G>A	XP_016866594.1:p.Arg1486=
XM_017011106.2:c.4329G>A	XP_016866595.1:p.Arg1443=
XM_017011107.2:c.4308G>A	XP_016866596.1:p.Arg1436=
XR_002956289.1:n.4603G>A
NM_001363725.2:c.2157G>A	NP_001350654.1:p.Arg719=
NM_001371656.1:c.4536G>A	NP_001358585.1:p.Arg1512=
NM_001374820.1:c.4536G>A	NP_001361749.1:p.Arg1512=
NM_001374828.1:c.4656G>A MANE Select	NP_001361757.1:p.Arg1552=
NM_017519.3:c.4497G>A	NP_059989.3:p.Arg1499=