Canonical Allele Identifier: CA452978242

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375526
• MyVariant Identifiers: chr6:g.157522396A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201262A>T , CM000668.2:g.157201262A>T	GRCh38
NC_000006.11:g.157522396A>T , CM000668.1:g.157522396A>T	GRCh37
NC_000006.10:g.157564088A>T	NCBI36
NG_032093.1:g.428333A>T
NG_032093.2:g.428333A>T
NG_066624.1:g.430237A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4878A>T	ENSP00000055163.8:p.Pro1626=
ENST00000414678.8:c.4947A>T	ENSP00000412835.3:p.Pro1649=
ENST00000637015.2:c.5166A>T	ENSP00000489729.2:p.Pro1722=
ENST00000346085.10:c.4917A>T	ENSP00000344546.5:p.Pro1639=
ENST00000350026.10:c.4629A>T	ENSP00000055163.7:p.Pro1543=
ENST00000414678.7:c.3195A>T	ENSP00000412835.2:p.Pro1065=
ENST00000635849.1:c.2358A>T	ENSP00000490948.1:p.Pro786=
ENST00000635957.1:c.1989A>T	ENSP00000490385.1:p.Pro663=
ENST00000636227.1:n.3500A>T
ENST00000636254.1:n.957A>T
ENST00000636930.2:c.5037A>T MANE Select	ENSP00000490491.2:p.Pro1679=
ENST00000636940.1:n.3034A>T
ENST00000637015.1:c.2405A>T
ENST00000637568.1:c.2319A>T
ENST00000637741.1:n.1703A>T
ENST00000637810.1:c.2379A>T	ENSP00000489636.1:p.Pro793=
ENST00000637904.1:c.2538A>T	ENSP00000490550.1:p.Pro846=
ENST00000647938.1:c.4668A>T	ENSP00000498155.1:p.Pro1556=
ENST00000346085.9:c.4668A>T	ENSP00000344546.4:p.Pro1556=
ENST00000350026.9:c.4629A>T	ENSP00000055163.7:p.Pro1543=
ENST00000414678.6:c.3195A>T	ENSP00000412835.2:p.Pro1065=
NM_017519.2:c.4629A>T	NP_059989.2:p.Pro1543=
NM_020732.3:c.4668A>T	NP_065783.3:p.Pro1556=
XM_005267069.3:c.4788A>T	XP_005267126.2:p.Pro1596=
XM_011535984.1:c.3867A>T	XP_011534286.1:p.Pro1289=
XM_011535985.1:c.3687A>T	XP_011534287.1:p.Pro1229=
XM_011535986.1:c.3447A>T	XP_011534288.1:p.Pro1149=
XM_011535987.1:c.3066A>T	XP_011534289.1:p.Pro1022=
XM_011535988.1:c.1929A>T	XP_011534290.1:p.Pro643=
NM_001346813.1:c.4788A>T	NP_001333742.1:p.Pro1596=
NM_001363725.1:c.2538A>T	NP_001350654.1:p.Pro846=
XM_011535984.2:c.4998A>T	XP_011534286.2:p.Pro1666=
XM_011535988.3:c.1929A>T	XP_011534290.1:p.Pro643=
XM_017011103.2:c.4899A>T	XP_016866592.1:p.Pro1633=
XM_017011104.1:c.4869A>T	XP_016866593.1:p.Pro1623=
XM_017011105.2:c.4839A>T	XP_016866594.1:p.Pro1613=
XM_017011106.2:c.4710A>T	XP_016866595.1:p.Pro1570=
XM_017011107.2:c.4689A>T	XP_016866596.1:p.Pro1563=
XR_002956289.1:n.4984A>T
NM_001363725.2:c.2538A>T	NP_001350654.1:p.Pro846=
NM_001371656.1:c.4917A>T	NP_001358585.1:p.Pro1639=
NM_001374820.1:c.4917A>T	NP_001361749.1:p.Pro1639=
NM_001374828.1:c.5037A>T MANE Select	NP_001361757.1:p.Pro1679=
NM_017519.3:c.4878A>T	NP_059989.3:p.Pro1626=