Canonical Allele Identifier: CA366241137

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522014G>A (hg19) ; chr6:g.157200880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200880G>A , CM000668.2:g.157200880G>A	GRCh38
NC_000006.11:g.157522014G>A , CM000668.1:g.157522014G>A	GRCh37
NC_000006.10:g.157563706G>A	NCBI36
NG_032093.1:g.427951G>A
NG_032093.2:g.427951G>A
NG_066624.1:g.429855G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4496G>A	ENSP00000055163.8:p.Arg1499Lys
ENST00000414678.8:c.4565G>A	ENSP00000412835.3:p.Arg1522Lys
ENST00000637015.2:c.4784G>A	ENSP00000489729.2:p.Arg1595Lys
ENST00000346085.10:c.4535G>A	ENSP00000344546.5:p.Arg1512Lys
ENST00000350026.10:c.4247G>A	ENSP00000055163.7:p.Arg1416Lys
ENST00000414678.7:c.2813G>A	ENSP00000412835.2:p.Arg938Lys
ENST00000635849.1:c.1976G>A	ENSP00000490948.1:p.Arg659Lys
ENST00000635957.1:c.1607G>A	ENSP00000490385.1:p.Arg536Lys
ENST00000636227.1:n.3118G>A
ENST00000636254.1:n.575G>A
ENST00000636930.2:c.4655G>A MANE Select	ENSP00000490491.2:p.Arg1552Lys
ENST00000636940.1:n.2652G>A
ENST00000637015.1:c.2023G>A
ENST00000637568.1:c.1937G>A
ENST00000637741.1:n.1321G>A
ENST00000637810.1:c.1997G>A	ENSP00000489636.1:p.Arg666Lys
ENST00000637904.1:c.2156G>A	ENSP00000490550.1:p.Arg719Lys
ENST00000647938.1:c.4286G>A	ENSP00000498155.1:p.Arg1429Lys
ENST00000346085.9:c.4286G>A	ENSP00000344546.4:p.Arg1429Lys
ENST00000350026.9:c.4247G>A	ENSP00000055163.7:p.Arg1416Lys
ENST00000414678.6:c.2813G>A	ENSP00000412835.2:p.Arg938Lys
NM_017519.2:c.4247G>A	NP_059989.2:p.Arg1416Lys
NM_020732.3:c.4286G>A	NP_065783.3:p.Arg1429Lys
XM_005267069.3:c.4406G>A	XP_005267126.2:p.Arg1469Lys
XM_011535984.1:c.3485G>A	XP_011534286.1:p.Arg1162Lys
XM_011535985.1:c.3305G>A	XP_011534287.1:p.Arg1102Lys
XM_011535986.1:c.3065G>A	XP_011534288.1:p.Arg1022Lys
XM_011535987.1:c.2684G>A	XP_011534289.1:p.Arg895Lys
XM_011535988.1:c.1547G>A	XP_011534290.1:p.Arg516Lys
NM_001346813.1:c.4406G>A	NP_001333742.1:p.Arg1469Lys
NM_001363725.1:c.2156G>A	NP_001350654.1:p.Arg719Lys
XM_011535984.2:c.4616G>A	XP_011534286.2:p.Arg1539Lys
XM_011535988.3:c.1547G>A	XP_011534290.1:p.Arg516Lys
XM_017011103.2:c.4517G>A	XP_016866592.1:p.Arg1506Lys
XM_017011104.1:c.4487G>A	XP_016866593.1:p.Arg1496Lys
XM_017011105.2:c.4457G>A	XP_016866594.1:p.Arg1486Lys
XM_017011106.2:c.4328G>A	XP_016866595.1:p.Arg1443Lys
XM_017011107.2:c.4307G>A	XP_016866596.1:p.Arg1436Lys
XR_002956289.1:n.4602G>A
NM_001363725.2:c.2156G>A	NP_001350654.1:p.Arg719Lys
NM_001371656.1:c.4535G>A	NP_001358585.1:p.Arg1512Lys
NM_001374820.1:c.4535G>A	NP_001361749.1:p.Arg1512Lys
NM_001374828.1:c.4655G>A MANE Select	NP_001361757.1:p.Arg1552Lys
NM_017519.3:c.4496G>A	NP_059989.3:p.Arg1499Lys