Canonical Allele Identifier: CA366242330

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522383G>T (hg19) ; chr6:g.157201249G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201249G>T , CM000668.2:g.157201249G>T	GRCh38
NC_000006.11:g.157522383G>T , CM000668.1:g.157522383G>T	GRCh37
NC_000006.10:g.157564075G>T	NCBI36
NG_032093.1:g.428320G>T
NG_032093.2:g.428320G>T
NG_066624.1:g.430224G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4865G>T	ENSP00000055163.8:p.Arg1622Met
ENST00000414678.8:c.4934G>T	ENSP00000412835.3:p.Arg1645Met
ENST00000637015.2:c.5153G>T	ENSP00000489729.2:p.Arg1718Met
ENST00000346085.10:c.4904G>T	ENSP00000344546.5:p.Arg1635Met
ENST00000350026.10:c.4616G>T	ENSP00000055163.7:p.Arg1539Met
ENST00000414678.7:c.3182G>T	ENSP00000412835.2:p.Arg1061Met
ENST00000635849.1:c.2345G>T	ENSP00000490948.1:p.Arg782Met
ENST00000635957.1:c.1976G>T	ENSP00000490385.1:p.Arg659Met
ENST00000636227.1:n.3487G>T
ENST00000636254.1:n.944G>T
ENST00000636930.2:c.5024G>T MANE Select	ENSP00000490491.2:p.Arg1675Met
ENST00000636940.1:n.3021G>T
ENST00000637015.1:c.2392G>T
ENST00000637568.1:c.2306G>T
ENST00000637741.1:n.1690G>T
ENST00000637810.1:c.2366G>T	ENSP00000489636.1:p.Arg789Met
ENST00000637904.1:c.2525G>T	ENSP00000490550.1:p.Arg842Met
ENST00000647938.1:c.4655G>T	ENSP00000498155.1:p.Arg1552Met
ENST00000346085.9:c.4655G>T	ENSP00000344546.4:p.Arg1552Met
ENST00000350026.9:c.4616G>T	ENSP00000055163.7:p.Arg1539Met
ENST00000414678.6:c.3182G>T	ENSP00000412835.2:p.Arg1061Met
NM_017519.2:c.4616G>T	NP_059989.2:p.Arg1539Met
NM_020732.3:c.4655G>T	NP_065783.3:p.Arg1552Met
XM_005267069.3:c.4775G>T	XP_005267126.2:p.Arg1592Met
XM_011535984.1:c.3854G>T	XP_011534286.1:p.Arg1285Met
XM_011535985.1:c.3674G>T	XP_011534287.1:p.Arg1225Met
XM_011535986.1:c.3434G>T	XP_011534288.1:p.Arg1145Met
XM_011535987.1:c.3053G>T	XP_011534289.1:p.Arg1018Met
XM_011535988.1:c.1916G>T	XP_011534290.1:p.Arg639Met
NM_001346813.1:c.4775G>T	NP_001333742.1:p.Arg1592Met
NM_001363725.1:c.2525G>T	NP_001350654.1:p.Arg842Met
XM_011535984.2:c.4985G>T	XP_011534286.2:p.Arg1662Met
XM_011535988.3:c.1916G>T	XP_011534290.1:p.Arg639Met
XM_017011103.2:c.4886G>T	XP_016866592.1:p.Arg1629Met
XM_017011104.1:c.4856G>T	XP_016866593.1:p.Arg1619Met
XM_017011105.2:c.4826G>T	XP_016866594.1:p.Arg1609Met
XM_017011106.2:c.4697G>T	XP_016866595.1:p.Arg1566Met
XM_017011107.2:c.4676G>T	XP_016866596.1:p.Arg1559Met
XR_002956289.1:n.4971G>T
NM_001363725.2:c.2525G>T	NP_001350654.1:p.Arg842Met
NM_001371656.1:c.4904G>T	NP_001358585.1:p.Arg1635Met
NM_001374820.1:c.4904G>T	NP_001361749.1:p.Arg1635Met
NM_001374828.1:c.5024G>T MANE Select	NP_001361757.1:p.Arg1675Met
NM_017519.3:c.4865G>T	NP_059989.3:p.Arg1622Met