Canonical Allele Identifier: CA366235044

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511216A>T (hg19) ; chr6:g.157190082A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190082A>T , CM000668.2:g.157190082A>T	GRCh38
NC_000006.11:g.157511216A>T , CM000668.1:g.157511216A>T	GRCh37
NC_000006.10:g.157552908A>T	NCBI36
NG_032093.1:g.417153A>T
NG_032093.2:g.417153A>T
NG_066624.1:g.419057A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3944A>T	ENSP00000055163.8:p.Asp1315Val
ENST00000414678.8:c.4013A>T	ENSP00000412835.3:p.Asp1338Val
ENST00000637015.2:c.4232A>T	ENSP00000489729.2:p.Asp1411Val
ENST00000346085.10:c.3983A>T	ENSP00000344546.5:p.Asp1328Val
ENST00000350026.10:c.3695A>T	ENSP00000055163.7:p.Asp1232Val
ENST00000414678.7:c.2261A>T	ENSP00000412835.2:p.Asp754Val
ENST00000635849.1:c.1424A>T	ENSP00000490948.1:p.Asp475Val
ENST00000635957.1:c.1055A>T	ENSP00000490385.1:p.Asp352Val
ENST00000636930.2:c.4103A>T MANE Select	ENSP00000490491.2:p.Asp1368Val
ENST00000636940.1:n.2100A>T
ENST00000637015.1:c.1471A>T
ENST00000637568.1:c.1385A>T
ENST00000637741.1:n.769A>T
ENST00000637810.1:c.1445A>T	ENSP00000489636.1:p.Asp482Val
ENST00000637904.1:c.1604A>T	ENSP00000490550.1:p.Asp535Val
ENST00000647938.1:c.3734A>T	ENSP00000498155.1:p.Asp1245Val
ENST00000346085.9:c.3734A>T	ENSP00000344546.4:p.Asp1245Val
ENST00000350026.9:c.3695A>T	ENSP00000055163.7:p.Asp1232Val
ENST00000414678.6:c.2261A>T	ENSP00000412835.2:p.Asp754Val
NM_017519.2:c.3695A>T	NP_059989.2:p.Asp1232Val
NM_020732.3:c.3734A>T	NP_065783.3:p.Asp1245Val
XM_005267069.3:c.3854A>T	XP_005267126.2:p.Asp1285Val
XM_011535984.1:c.2933A>T	XP_011534286.1:p.Asp978Val
XM_011535985.1:c.2753A>T	XP_011534287.1:p.Asp918Val
XM_011535986.1:c.2513A>T	XP_011534288.1:p.Asp838Val
XM_011535987.1:c.2132A>T	XP_011534289.1:p.Asp711Val
XM_011535988.1:c.995A>T	XP_011534290.1:p.Asp332Val
NM_001346813.1:c.3854A>T	NP_001333742.1:p.Asp1285Val
NM_001363725.1:c.1604A>T	NP_001350654.1:p.Asp535Val
XM_011535984.2:c.4064A>T	XP_011534286.2:p.Asp1355Val
XM_011535988.3:c.995A>T	XP_011534290.1:p.Asp332Val
XM_017011103.2:c.3965A>T	XP_016866592.1:p.Asp1322Val
XM_017011104.1:c.3935A>T	XP_016866593.1:p.Asp1312Val
XM_017011105.2:c.3905A>T	XP_016866594.1:p.Asp1302Val
XM_017011106.2:c.3776A>T	XP_016866595.1:p.Asp1259Val
XM_017011107.2:c.3755A>T	XP_016866596.1:p.Asp1252Val
XR_002956289.1:n.4147A>T
NM_001363725.2:c.1604A>T	NP_001350654.1:p.Asp535Val
NM_001371656.1:c.3983A>T	NP_001358585.1:p.Asp1328Val
NM_001374820.1:c.3983A>T	NP_001361749.1:p.Asp1328Val
NM_001374828.1:c.4103A>T MANE Select	NP_001361757.1:p.Asp1368Val
NM_017519.3:c.3944A>T	NP_059989.3:p.Asp1315Val