Canonical Allele Identifier: CA2563391781

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128211036

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901502del , CM000668.2:g.156901502del	GRCh38
NC_000006.11:g.157222636del , CM000668.1:g.157222636del	GRCh37
NC_000006.10:g.157264328del	NCBI36
NG_032093.1:g.128573del
NG_032093.2:g.128573del
NG_066624.1:g.130477del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2113del	ENSP00000055163.8:p.Gln705SerfsTer?
ENST00000414678.8:c.2113del	ENSP00000412835.3:p.Gln705SerfsTer?
ENST00000637015.2:c.2113del	ENSP00000489729.2:p.Gln705SerfsTer?
ENST00000319584.11:c.127del	ENSP00000313006.7:p.Gln43SerfsTer?
ENST00000346085.10:c.2152del	ENSP00000344546.5:p.Gln718SerfsTer?
ENST00000350026.10:c.1864del	ENSP00000055163.7:p.Gln622SerfsTer?
ENST00000414678.7:c.361del	ENSP00000412835.2:p.Gln121SerfsTer?
ENST00000636205.1:n.176del
ENST00000636748.1:c.394del	ENSP00000489917.1:p.Gln132SerfsTer?
ENST00000636930.2:c.2113del MANE Select	ENSP00000490491.2:p.Gln705SerfsTer?
ENST00000637532.1:c.139del	ENSP00000490420.1:p.Gln47SerfsTer?
ENST00000638000.1:c.330del
ENST00000647938.1:c.1903del	ENSP00000498155.1:p.Gln635SerfsTer?
ENST00000674190.1:n.820del
ENST00000674298.1:c.1853del
ENST00000319584.10:c.130del	ENSP00000313006.6:p.Gln44SerfsTer?
ENST00000346085.9:c.1903del	ENSP00000344546.4:p.Gln635SerfsTer?
ENST00000350026.9:c.1864del	ENSP00000055163.7:p.Gln622SerfsTer?
ENST00000414678.6:c.361del	ENSP00000412835.2:p.Gln121SerfsTer?
NM_017519.2:c.1864del	NP_059989.2:p.Gln622SerfsTer?
NM_020732.3:c.1903del	NP_065783.3:p.Gln635SerfsTer?
XM_005267069.3:c.1864del	XP_005267126.2:p.Gln622SerfsTer?
XM_011535984.1:c.772del	XP_011534286.1:p.Gln258SerfsTer?
XM_011535985.1:c.772del	XP_011534287.1:p.Gln258SerfsTer?
XM_011535986.1:c.352del	XP_011534288.1:p.Gln118SerfsTer?
NM_001346813.1:c.1864del	NP_001333742.1:p.Gln622SerfsTer?
XM_011535984.2:c.1903del	XP_011534286.2:p.Gln635SerfsTer?
XM_017011103.2:c.1903del	XP_016866592.1:p.Gln635SerfsTer?
XM_017011104.1:c.1903del	XP_016866593.1:p.Gln635SerfsTer?
XM_017011105.2:c.1903del	XP_016866594.1:p.Gln635SerfsTer?
XM_017011106.2:c.1903del	XP_016866595.1:p.Gln635SerfsTer?
XM_017011107.2:c.1903del	XP_016866596.1:p.Gln635SerfsTer?
XR_002956289.1:n.1986del
NM_001371656.1:c.2152del	NP_001358585.1:p.Gln718SerfsTer?
NM_001374820.1:c.2152del	NP_001361749.1:p.Gln718SerfsTer?
NM_001374828.1:c.2113del MANE Select	NP_001361757.1:p.Gln705SerfsTer?
NM_017519.3:c.2113del	NP_059989.3:p.Gln705SerfsTer?