Canonical Allele Identifier: CA366234849

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511195A>T (hg19) ; chr6:g.157190061A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190061A>T , CM000668.2:g.157190061A>T	GRCh38
NC_000006.11:g.157511195A>T , CM000668.1:g.157511195A>T	GRCh37
NC_000006.10:g.157552887A>T	NCBI36
NG_032093.1:g.417132A>T
NG_032093.2:g.417132A>T
NG_066624.1:g.419036A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3923A>T	ENSP00000055163.8:p.Asp1308Val
ENST00000414678.8:c.3992A>T	ENSP00000412835.3:p.Asp1331Val
ENST00000637015.2:c.4211A>T	ENSP00000489729.2:p.Asp1404Val
ENST00000346085.10:c.3962A>T	ENSP00000344546.5:p.Asp1321Val
ENST00000350026.10:c.3674A>T	ENSP00000055163.7:p.Asp1225Val
ENST00000414678.7:c.2240A>T	ENSP00000412835.2:p.Asp747Val
ENST00000635849.1:c.1403A>T	ENSP00000490948.1:p.Asp468Val
ENST00000635957.1:c.1034A>T	ENSP00000490385.1:p.Asp345Val
ENST00000636930.2:c.4082A>T MANE Select	ENSP00000490491.2:p.Asp1361Val
ENST00000636940.1:n.2079A>T
ENST00000637015.1:c.1450A>T
ENST00000637568.1:c.1364A>T
ENST00000637741.1:n.748A>T
ENST00000637810.1:c.1424A>T	ENSP00000489636.1:p.Asp475Val
ENST00000637904.1:c.1583A>T	ENSP00000490550.1:p.Asp528Val
ENST00000647938.1:c.3713A>T	ENSP00000498155.1:p.Asp1238Val
ENST00000346085.9:c.3713A>T	ENSP00000344546.4:p.Asp1238Val
ENST00000350026.9:c.3674A>T	ENSP00000055163.7:p.Asp1225Val
ENST00000414678.6:c.2240A>T	ENSP00000412835.2:p.Asp747Val
NM_017519.2:c.3674A>T	NP_059989.2:p.Asp1225Val
NM_020732.3:c.3713A>T	NP_065783.3:p.Asp1238Val
XM_005267069.3:c.3833A>T	XP_005267126.2:p.Asp1278Val
XM_011535984.1:c.2912A>T	XP_011534286.1:p.Asp971Val
XM_011535985.1:c.2732A>T	XP_011534287.1:p.Asp911Val
XM_011535986.1:c.2492A>T	XP_011534288.1:p.Asp831Val
XM_011535987.1:c.2111A>T	XP_011534289.1:p.Asp704Val
XM_011535988.1:c.974A>T	XP_011534290.1:p.Asp325Val
NM_001346813.1:c.3833A>T	NP_001333742.1:p.Asp1278Val
NM_001363725.1:c.1583A>T	NP_001350654.1:p.Asp528Val
XM_011535984.2:c.4043A>T	XP_011534286.2:p.Asp1348Val
XM_011535988.3:c.974A>T	XP_011534290.1:p.Asp325Val
XM_017011103.2:c.3944A>T	XP_016866592.1:p.Asp1315Val
XM_017011104.1:c.3914A>T	XP_016866593.1:p.Asp1305Val
XM_017011105.2:c.3884A>T	XP_016866594.1:p.Asp1295Val
XM_017011106.2:c.3755A>T	XP_016866595.1:p.Asp1252Val
XM_017011107.2:c.3734A>T	XP_016866596.1:p.Asp1245Val
XR_002956289.1:n.4126A>T
NM_001363725.2:c.1583A>T	NP_001350654.1:p.Asp528Val
NM_001371656.1:c.3962A>T	NP_001358585.1:p.Asp1321Val
NM_001374820.1:c.3962A>T	NP_001361749.1:p.Asp1321Val
NM_001374828.1:c.4082A>T MANE Select	NP_001361757.1:p.Asp1361Val
NM_017519.3:c.3923A>T	NP_059989.3:p.Asp1308Val