Canonical Allele Identifier: CA366234959

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511208T>A (hg19) ; chr6:g.157190074T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190074T>A , CM000668.2:g.157190074T>A	GRCh38
NC_000006.11:g.157511208T>A , CM000668.1:g.157511208T>A	GRCh37
NC_000006.10:g.157552900T>A	NCBI36
NG_032093.1:g.417145T>A
NG_032093.2:g.417145T>A
NG_066624.1:g.419049T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3936T>A	ENSP00000055163.8:p.Asp1312Glu
ENST00000414678.8:c.4005T>A	ENSP00000412835.3:p.Asp1335Glu
ENST00000637015.2:c.4224T>A	ENSP00000489729.2:p.Asp1408Glu
ENST00000346085.10:c.3975T>A	ENSP00000344546.5:p.Asp1325Glu
ENST00000350026.10:c.3687T>A	ENSP00000055163.7:p.Asp1229Glu
ENST00000414678.7:c.2253T>A	ENSP00000412835.2:p.Asp751Glu
ENST00000635849.1:c.1416T>A	ENSP00000490948.1:p.Asp472Glu
ENST00000635957.1:c.1047T>A	ENSP00000490385.1:p.Asp349Glu
ENST00000636930.2:c.4095T>A MANE Select	ENSP00000490491.2:p.Asp1365Glu
ENST00000636940.1:n.2092T>A
ENST00000637015.1:c.1463T>A
ENST00000637568.1:c.1377T>A
ENST00000637741.1:n.761T>A
ENST00000637810.1:c.1437T>A	ENSP00000489636.1:p.Asp479Glu
ENST00000637904.1:c.1596T>A	ENSP00000490550.1:p.Asp532Glu
ENST00000647938.1:c.3726T>A	ENSP00000498155.1:p.Asp1242Glu
ENST00000346085.9:c.3726T>A	ENSP00000344546.4:p.Asp1242Glu
ENST00000350026.9:c.3687T>A	ENSP00000055163.7:p.Asp1229Glu
ENST00000414678.6:c.2253T>A	ENSP00000412835.2:p.Asp751Glu
NM_017519.2:c.3687T>A	NP_059989.2:p.Asp1229Glu
NM_020732.3:c.3726T>A	NP_065783.3:p.Asp1242Glu
XM_005267069.3:c.3846T>A	XP_005267126.2:p.Asp1282Glu
XM_011535984.1:c.2925T>A	XP_011534286.1:p.Asp975Glu
XM_011535985.1:c.2745T>A	XP_011534287.1:p.Asp915Glu
XM_011535986.1:c.2505T>A	XP_011534288.1:p.Asp835Glu
XM_011535987.1:c.2124T>A	XP_011534289.1:p.Asp708Glu
XM_011535988.1:c.987T>A	XP_011534290.1:p.Asp329Glu
NM_001346813.1:c.3846T>A	NP_001333742.1:p.Asp1282Glu
NM_001363725.1:c.1596T>A	NP_001350654.1:p.Asp532Glu
XM_011535984.2:c.4056T>A	XP_011534286.2:p.Asp1352Glu
XM_011535988.3:c.987T>A	XP_011534290.1:p.Asp329Glu
XM_017011103.2:c.3957T>A	XP_016866592.1:p.Asp1319Glu
XM_017011104.1:c.3927T>A	XP_016866593.1:p.Asp1309Glu
XM_017011105.2:c.3897T>A	XP_016866594.1:p.Asp1299Glu
XM_017011106.2:c.3768T>A	XP_016866595.1:p.Asp1256Glu
XM_017011107.2:c.3747T>A	XP_016866596.1:p.Asp1249Glu
XR_002956289.1:n.4139T>A
NM_001363725.2:c.1596T>A	NP_001350654.1:p.Asp532Glu
NM_001371656.1:c.3975T>A	NP_001358585.1:p.Asp1325Glu
NM_001374820.1:c.3975T>A	NP_001361749.1:p.Asp1325Glu
NM_001374828.1:c.4095T>A MANE Select	NP_001361757.1:p.Asp1365Glu
NM_017519.3:c.3936T>A	NP_059989.3:p.Asp1312Glu