Canonical Allele Identifier: CA452781573

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510900A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189766A>T , CM000668.2:g.157189766A>T	GRCh38
NC_000006.11:g.157510900A>T , CM000668.1:g.157510900A>T	GRCh37
NC_000006.10:g.157552592A>T	NCBI36
NG_032093.1:g.416837A>T
NG_032093.2:g.416837A>T
NG_066624.1:g.418741A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3885A>T	ENSP00000055163.8:p.Pro1295=
ENST00000414678.8:c.3954A>T	ENSP00000412835.3:p.Pro1318=
ENST00000637015.2:c.4173A>T	ENSP00000489729.2:p.Pro1391=
ENST00000346085.10:c.3924A>T	ENSP00000344546.5:p.Pro1308=
ENST00000350026.10:c.3636A>T	ENSP00000055163.7:p.Pro1212=
ENST00000414678.7:c.2202A>T	ENSP00000412835.2:p.Pro734=
ENST00000635849.1:c.1365A>T	ENSP00000490948.1:p.Pro455=
ENST00000635957.1:c.999A>T	ENSP00000490385.1:p.Pro333=
ENST00000636930.2:c.4044A>T MANE Select	ENSP00000490491.2:p.Pro1348=
ENST00000636940.1:n.2041A>T
ENST00000637015.1:c.1412A>T
ENST00000637568.1:c.1326A>T
ENST00000637741.1:n.710A>T
ENST00000637810.1:c.1386A>T	ENSP00000489636.1:p.Pro462=
ENST00000637904.1:c.1545A>T	ENSP00000490550.1:p.Pro515=
ENST00000647938.1:c.3675A>T	ENSP00000498155.1:p.Pro1225=
ENST00000346085.9:c.3675A>T	ENSP00000344546.4:p.Pro1225=
ENST00000350026.9:c.3636A>T	ENSP00000055163.7:p.Pro1212=
ENST00000414678.6:c.2202A>T	ENSP00000412835.2:p.Pro734=
NM_017519.2:c.3636A>T	NP_059989.2:p.Pro1212=
NM_020732.3:c.3675A>T	NP_065783.3:p.Pro1225=
XM_005267069.3:c.3795A>T	XP_005267126.2:p.Pro1265=
XM_011535984.1:c.2874A>T	XP_011534286.1:p.Pro958=
XM_011535985.1:c.2694A>T	XP_011534287.1:p.Pro898=
XM_011535986.1:c.2454A>T	XP_011534288.1:p.Pro818=
XM_011535987.1:c.2073A>T	XP_011534289.1:p.Pro691=
XM_011535988.1:c.936A>T	XP_011534290.1:p.Pro312=
NM_001346813.1:c.3795A>T	NP_001333742.1:p.Pro1265=
NM_001363725.1:c.1545A>T	NP_001350654.1:p.Pro515=
XM_011535984.2:c.4005A>T	XP_011534286.2:p.Pro1335=
XM_011535988.3:c.936A>T	XP_011534290.1:p.Pro312=
XM_017011103.2:c.3906A>T	XP_016866592.1:p.Pro1302=
XM_017011104.1:c.3876A>T	XP_016866593.1:p.Pro1292=
XM_017011105.2:c.3846A>T	XP_016866594.1:p.Pro1282=
XM_017011106.2:c.3717A>T	XP_016866595.1:p.Pro1239=
XM_017011107.2:c.3696A>T	XP_016866596.1:p.Pro1232=
XR_002956289.1:n.4088A>T
NM_001363725.2:c.1545A>T	NP_001350654.1:p.Pro515=
NM_001371656.1:c.3924A>T	NP_001358585.1:p.Pro1308=
NM_001374820.1:c.3924A>T	NP_001361749.1:p.Pro1308=
NM_001374828.1:c.4044A>T MANE Select	NP_001361757.1:p.Pro1348=
NM_017519.3:c.3885A>T	NP_059989.3:p.Pro1295=