Canonical Allele Identifier: CA366241139

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4496G>T	ENSP00000055163.8:p.Arg1499Met
ENST00000414678.8:c.4565G>T	ENSP00000412835.3:p.Arg1522Met
ENST00000637015.2:c.4784G>T	ENSP00000489729.2:p.Arg1595Met
ENST00000346085.10:c.4535G>T	ENSP00000344546.5:p.Arg1512Met
ENST00000350026.10:c.4247G>T	ENSP00000055163.7:p.Arg1416Met
ENST00000414678.7:c.2813G>T	ENSP00000412835.2:p.Arg938Met
ENST00000635849.1:c.1976G>T	ENSP00000490948.1:p.Arg659Met
ENST00000635957.1:c.1607G>T	ENSP00000490385.1:p.Arg536Met
ENST00000636227.1:n.3118G>T
ENST00000636254.1:n.575G>T
ENST00000636930.2:c.4655G>T MANE Select	ENSP00000490491.2:p.Arg1552Met
ENST00000636940.1:n.2652G>T
ENST00000637015.1:c.2023G>T
ENST00000637568.1:c.1937G>T
ENST00000637741.1:n.1321G>T
ENST00000637810.1:c.1997G>T	ENSP00000489636.1:p.Arg666Met
ENST00000637904.1:c.2156G>T	ENSP00000490550.1:p.Arg719Met
ENST00000647938.1:c.4286G>T	ENSP00000498155.1:p.Arg1429Met
ENST00000346085.9:c.4286G>T	ENSP00000344546.4:p.Arg1429Met
ENST00000350026.9:c.4247G>T	ENSP00000055163.7:p.Arg1416Met
ENST00000414678.6:c.2813G>T	ENSP00000412835.2:p.Arg938Met
NM_017519.2:c.4247G>T	NP_059989.2:p.Arg1416Met
NM_020732.3:c.4286G>T	NP_065783.3:p.Arg1429Met
XM_005267069.3:c.4406G>T	XP_005267126.2:p.Arg1469Met
XM_011535984.1:c.3485G>T	XP_011534286.1:p.Arg1162Met
XM_011535985.1:c.3305G>T	XP_011534287.1:p.Arg1102Met
XM_011535986.1:c.3065G>T	XP_011534288.1:p.Arg1022Met
XM_011535987.1:c.2684G>T	XP_011534289.1:p.Arg895Met
XM_011535988.1:c.1547G>T	XP_011534290.1:p.Arg516Met
NM_001346813.1:c.4406G>T	NP_001333742.1:p.Arg1469Met
NM_001363725.1:c.2156G>T	NP_001350654.1:p.Arg719Met
XM_011535984.2:c.4616G>T	XP_011534286.2:p.Arg1539Met
XM_011535988.3:c.1547G>T	XP_011534290.1:p.Arg516Met
XM_017011103.2:c.4517G>T	XP_016866592.1:p.Arg1506Met
XM_017011104.1:c.4487G>T	XP_016866593.1:p.Arg1496Met
XM_017011105.2:c.4457G>T	XP_016866594.1:p.Arg1486Met
XM_017011106.2:c.4328G>T	XP_016866595.1:p.Arg1443Met
XM_017011107.2:c.4307G>T	XP_016866596.1:p.Arg1436Met
XR_002956289.1:n.4602G>T
NM_001363725.2:c.2156G>T	NP_001350654.1:p.Arg719Met
NM_001371656.1:c.4535G>T	NP_001358585.1:p.Arg1512Met
NM_001374820.1:c.4535G>T	NP_001361749.1:p.Arg1512Met
NM_001374828.1:c.4655G>T MANE Select	NP_001361757.1:p.Arg1552Met
NM_017519.3:c.4496G>T	NP_059989.3:p.Arg1499Met