Canonical Allele Identifier: CA366242063

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522262T>A (hg19) ; chr6:g.157201128T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201128T>A , CM000668.2:g.157201128T>A	GRCh38
NC_000006.11:g.157522262T>A , CM000668.1:g.157522262T>A	GRCh37
NC_000006.10:g.157563954T>A	NCBI36
NG_032093.1:g.428199T>A
NG_032093.2:g.428199T>A
NG_066624.1:g.430103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4744T>A	ENSP00000055163.8:p.Trp1582Arg
ENST00000414678.8:c.4813T>A	ENSP00000412835.3:p.Trp1605Arg
ENST00000637015.2:c.5032T>A	ENSP00000489729.2:p.Trp1678Arg
ENST00000346085.10:c.4783T>A	ENSP00000344546.5:p.Trp1595Arg
ENST00000350026.10:c.4495T>A	ENSP00000055163.7:p.Trp1499Arg
ENST00000414678.7:c.3061T>A	ENSP00000412835.2:p.Trp1021Arg
ENST00000635849.1:c.2224T>A	ENSP00000490948.1:p.Trp742Arg
ENST00000635957.1:c.1855T>A	ENSP00000490385.1:p.Trp619Arg
ENST00000636227.1:n.3366T>A
ENST00000636254.1:n.823T>A
ENST00000636930.2:c.4903T>A MANE Select	ENSP00000490491.2:p.Trp1635Arg
ENST00000636940.1:n.2900T>A
ENST00000637015.1:c.2271T>A
ENST00000637568.1:c.2185T>A
ENST00000637741.1:n.1569T>A
ENST00000637810.1:c.2245T>A	ENSP00000489636.1:p.Trp749Arg
ENST00000637904.1:c.2404T>A	ENSP00000490550.1:p.Trp802Arg
ENST00000647938.1:c.4534T>A	ENSP00000498155.1:p.Trp1512Arg
ENST00000346085.9:c.4534T>A	ENSP00000344546.4:p.Trp1512Arg
ENST00000350026.9:c.4495T>A	ENSP00000055163.7:p.Trp1499Arg
ENST00000414678.6:c.3061T>A	ENSP00000412835.2:p.Trp1021Arg
NM_017519.2:c.4495T>A	NP_059989.2:p.Trp1499Arg
NM_020732.3:c.4534T>A	NP_065783.3:p.Trp1512Arg
XM_005267069.3:c.4654T>A	XP_005267126.2:p.Trp1552Arg
XM_011535984.1:c.3733T>A	XP_011534286.1:p.Trp1245Arg
XM_011535985.1:c.3553T>A	XP_011534287.1:p.Trp1185Arg
XM_011535986.1:c.3313T>A	XP_011534288.1:p.Trp1105Arg
XM_011535987.1:c.2932T>A	XP_011534289.1:p.Trp978Arg
XM_011535988.1:c.1795T>A	XP_011534290.1:p.Trp599Arg
NM_001346813.1:c.4654T>A	NP_001333742.1:p.Trp1552Arg
NM_001363725.1:c.2404T>A	NP_001350654.1:p.Trp802Arg
XM_011535984.2:c.4864T>A	XP_011534286.2:p.Trp1622Arg
XM_011535988.3:c.1795T>A	XP_011534290.1:p.Trp599Arg
XM_017011103.2:c.4765T>A	XP_016866592.1:p.Trp1589Arg
XM_017011104.1:c.4735T>A	XP_016866593.1:p.Trp1579Arg
XM_017011105.2:c.4705T>A	XP_016866594.1:p.Trp1569Arg
XM_017011106.2:c.4576T>A	XP_016866595.1:p.Trp1526Arg
XM_017011107.2:c.4555T>A	XP_016866596.1:p.Trp1519Arg
XR_002956289.1:n.4850T>A
NM_001363725.2:c.2404T>A	NP_001350654.1:p.Trp802Arg
NM_001371656.1:c.4783T>A	NP_001358585.1:p.Trp1595Arg
NM_001374820.1:c.4783T>A	NP_001361749.1:p.Trp1595Arg
NM_001374828.1:c.4903T>A MANE Select	NP_001361757.1:p.Trp1635Arg
NM_017519.3:c.4744T>A	NP_059989.3:p.Trp1582Arg