Canonical Allele Identifier: CA2580075253

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1706377
• ClinVar RCV Id: RCV002284907

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901515_156901516delinsGC , CM000668.2:g.156901515_156901516delinsGC	GRCh38
NC_000006.11:g.157222649_157222650delinsGC , CM000668.1:g.157222649_157222650delinsGC	GRCh37
NC_000006.10:g.157264341_157264342delinsGC	NCBI36
NG_032093.1:g.128586_128587delinsGC
NG_032093.2:g.128586_128587delinsGC
NG_066624.1:g.130490_130491delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2126_2127delinsGC	ENSP00000055163.8:p.Gln709Arg
ENST00000414678.8:c.2126_2127delinsGC	ENSP00000412835.3:p.Gln709Arg
ENST00000637015.2:c.2126_2127delinsGC	ENSP00000489729.2:p.Gln709Arg
ENST00000319584.11:c.140_141delinsGC	ENSP00000313006.7:p.Gln47Arg
ENST00000346085.10:c.2165_2166delinsGC	ENSP00000344546.5:p.Gln722Arg
ENST00000350026.10:c.1877_1878delinsGC	ENSP00000055163.7:p.Gln626Arg
ENST00000414678.7:c.374_375delinsGC	ENSP00000412835.2:p.Gln125Arg
ENST00000636205.1:n.189_190delinsGC
ENST00000636748.1:c.407_408delinsGC	ENSP00000489917.1:p.Gln136Arg
ENST00000636930.2:c.2126_2127delinsGC MANE Select	ENSP00000490491.2:p.Gln709Arg
ENST00000637532.1:c.152_153delinsGC	ENSP00000490420.1:p.Gln51Arg
ENST00000638000.1:c.343_344delinsGC
ENST00000647938.1:c.1916_1917delinsGC	ENSP00000498155.1:p.Gln639Arg
ENST00000674190.1:n.833_834delinsGC
ENST00000674298.1:c.1866_1867delinsGC
ENST00000319584.10:c.143_144delinsGC	ENSP00000313006.6:p.Gln48Arg
ENST00000346085.9:c.1916_1917delinsGC	ENSP00000344546.4:p.Gln639Arg
ENST00000350026.9:c.1877_1878delinsGC	ENSP00000055163.7:p.Gln626Arg
ENST00000414678.6:c.374_375delinsGC	ENSP00000412835.2:p.Gln125Arg
NM_017519.2:c.1877_1878delinsGC	NP_059989.2:p.Gln626Arg
NM_020732.3:c.1916_1917delinsGC	NP_065783.3:p.Gln639Arg
XM_005267069.3:c.1877_1878delinsGC	XP_005267126.2:p.Gln626Arg
XM_011535984.1:c.785_786delinsGC	XP_011534286.1:p.Gln262Arg
XM_011535985.1:c.785_786delinsGC	XP_011534287.1:p.Gln262Arg
XM_011535986.1:c.365_366delinsGC	XP_011534288.1:p.Gln122Arg
NM_001346813.1:c.1877_1878delinsGC	NP_001333742.1:p.Gln626Arg
XM_011535984.2:c.1916_1917delinsGC	XP_011534286.2:p.Gln639Arg
XM_017011103.2:c.1916_1917delinsGC	XP_016866592.1:p.Gln639Arg
XM_017011104.1:c.1916_1917delinsGC	XP_016866593.1:p.Gln639Arg
XM_017011105.2:c.1916_1917delinsGC	XP_016866594.1:p.Gln639Arg
XM_017011106.2:c.1916_1917delinsGC	XP_016866595.1:p.Gln639Arg
XM_017011107.2:c.1916_1917delinsGC	XP_016866596.1:p.Gln639Arg
XR_002956289.1:n.1999_2000delinsGC
NM_001371656.1:c.2165_2166delinsGC	NP_001358585.1:p.Gln722Arg
NM_001374820.1:c.2165_2166delinsGC	NP_001361749.1:p.Gln722Arg
NM_001374828.1:c.2126_2127delinsGC MANE Select	NP_001361757.1:p.Gln709Arg
NM_017519.3:c.2126_2127delinsGC	NP_059989.3:p.Gln709Arg