Canonical Allele Identifier: CA452781898

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511250A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190116A>T , CM000668.2:g.157190116A>T	GRCh38
NC_000006.11:g.157511250A>T , CM000668.1:g.157511250A>T	GRCh37
NC_000006.10:g.157552942A>T	NCBI36
NG_032093.1:g.417187A>T
NG_032093.2:g.417187A>T
NG_066624.1:g.419091A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3978A>T	ENSP00000055163.8:p.Pro1326=
ENST00000414678.8:c.4047A>T	ENSP00000412835.3:p.Pro1349=
ENST00000637015.2:c.4266A>T	ENSP00000489729.2:p.Pro1422=
ENST00000346085.10:c.4017A>T	ENSP00000344546.5:p.Pro1339=
ENST00000350026.10:c.3729A>T	ENSP00000055163.7:p.Pro1243=
ENST00000414678.7:c.2295A>T	ENSP00000412835.2:p.Pro765=
ENST00000635849.1:c.1458A>T	ENSP00000490948.1:p.Pro486=
ENST00000635957.1:c.1089A>T	ENSP00000490385.1:p.Pro363=
ENST00000636930.2:c.4137A>T MANE Select	ENSP00000490491.2:p.Pro1379=
ENST00000636940.1:n.2134A>T
ENST00000637015.1:c.1505A>T
ENST00000637568.1:c.1419A>T
ENST00000637741.1:n.803A>T
ENST00000637810.1:c.1479A>T	ENSP00000489636.1:p.Pro493=
ENST00000637904.1:c.1638A>T	ENSP00000490550.1:p.Pro546=
ENST00000647938.1:c.3768A>T	ENSP00000498155.1:p.Pro1256=
ENST00000346085.9:c.3768A>T	ENSP00000344546.4:p.Pro1256=
ENST00000350026.9:c.3729A>T	ENSP00000055163.7:p.Pro1243=
ENST00000414678.6:c.2295A>T	ENSP00000412835.2:p.Pro765=
NM_017519.2:c.3729A>T	NP_059989.2:p.Pro1243=
NM_020732.3:c.3768A>T	NP_065783.3:p.Pro1256=
XM_005267069.3:c.3888A>T	XP_005267126.2:p.Pro1296=
XM_011535984.1:c.2967A>T	XP_011534286.1:p.Pro989=
XM_011535985.1:c.2787A>T	XP_011534287.1:p.Pro929=
XM_011535986.1:c.2547A>T	XP_011534288.1:p.Pro849=
XM_011535987.1:c.2166A>T	XP_011534289.1:p.Pro722=
XM_011535988.1:c.1029A>T	XP_011534290.1:p.Pro343=
NM_001346813.1:c.3888A>T	NP_001333742.1:p.Pro1296=
NM_001363725.1:c.1638A>T	NP_001350654.1:p.Pro546=
XM_011535984.2:c.4098A>T	XP_011534286.2:p.Pro1366=
XM_011535988.3:c.1029A>T	XP_011534290.1:p.Pro343=
XM_017011103.2:c.3999A>T	XP_016866592.1:p.Pro1333=
XM_017011104.1:c.3969A>T	XP_016866593.1:p.Pro1323=
XM_017011105.2:c.3939A>T	XP_016866594.1:p.Pro1313=
XM_017011106.2:c.3810A>T	XP_016866595.1:p.Pro1270=
XM_017011107.2:c.3789A>T	XP_016866596.1:p.Pro1263=
XR_002956289.1:n.4181A>T
NM_001363725.2:c.1638A>T	NP_001350654.1:p.Pro546=
NM_001371656.1:c.4017A>T	NP_001358585.1:p.Pro1339=
NM_001374820.1:c.4017A>T	NP_001361749.1:p.Pro1339=
NM_001374828.1:c.4137A>T MANE Select	NP_001361757.1:p.Pro1379=
NM_017519.3:c.3978A>T	NP_059989.3:p.Pro1326=