Canonical Allele Identifier: CA366228426

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231267
• MyVariant Identifiers: chr6:g.157502292G>T (hg19) ; chr6:g.157181158G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181158G>T , CM000668.2:g.157181158G>T	GRCh38
NC_000006.11:g.157502292G>T , CM000668.1:g.157502292G>T	GRCh37
NC_000006.10:g.157543984G>T	NCBI36
NG_032093.1:g.408229G>T
NG_032093.2:g.408229G>T
NG_066624.1:g.410133G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3535G>T	ENSP00000055163.8:p.Glu1179Ter
ENST00000414678.8:c.3604G>T	ENSP00000412835.3:p.Glu1202Ter
ENST00000637015.2:c.3823G>T	ENSP00000489729.2:p.Glu1275Ter
ENST00000319584.11:c.1708G>T	ENSP00000313006.7:p.Glu570Ter
ENST00000346085.10:c.3574G>T	ENSP00000344546.5:p.Glu1192Ter
ENST00000350026.10:c.3286G>T	ENSP00000055163.7:p.Glu1096Ter
ENST00000414678.7:c.1852G>T	ENSP00000412835.2:p.Glu618Ter
ENST00000635849.1:c.1015G>T	ENSP00000490948.1:p.Glu339Ter
ENST00000635957.1:c.649G>T	ENSP00000490385.1:p.Glu217Ter
ENST00000636930.2:c.3694G>T MANE Select	ENSP00000490491.2:p.Glu1232Ter
ENST00000636940.1:n.1691G>T
ENST00000637015.1:c.1062G>T
ENST00000637568.1:c.976G>T
ENST00000637741.1:n.360G>T
ENST00000637810.1:c.1036G>T	ENSP00000489636.1:p.Glu346Ter
ENST00000637904.1:c.1195G>T	ENSP00000490550.1:p.Glu399Ter
ENST00000647938.1:c.3325G>T	ENSP00000498155.1:p.Glu1109Ter
ENST00000319584.10:c.1711G>T	ENSP00000313006.6:p.Glu571Ter
ENST00000346085.9:c.3325G>T	ENSP00000344546.4:p.Glu1109Ter
ENST00000350026.9:c.3286G>T	ENSP00000055163.7:p.Glu1096Ter
ENST00000400790.3:c.487G>T	ENSP00000383596.3:p.Glu163Ter
ENST00000414678.6:c.1852G>T	ENSP00000412835.2:p.Glu618Ter
ENST00000478761.3:c.896G>T
NM_017519.2:c.3286G>T	NP_059989.2:p.Glu1096Ter
NM_020732.3:c.3325G>T	NP_065783.3:p.Glu1109Ter
XM_005267069.3:c.3445G>T	XP_005267126.2:p.Glu1149Ter
XM_011535984.1:c.2524G>T	XP_011534286.1:p.Glu842Ter
XM_011535985.1:c.2344G>T	XP_011534287.1:p.Glu782Ter
XM_011535986.1:c.2104G>T	XP_011534288.1:p.Glu702Ter
XM_011535987.1:c.1723G>T	XP_011534289.1:p.Glu575Ter
XM_011535988.1:c.586G>T	XP_011534290.1:p.Glu196Ter
NM_001346813.1:c.3445G>T	NP_001333742.1:p.Glu1149Ter
NM_001363725.1:c.1195G>T	NP_001350654.1:p.Glu399Ter
XM_011535984.2:c.3655G>T	XP_011534286.2:p.Glu1219Ter
XM_011535988.3:c.586G>T	XP_011534290.1:p.Glu196Ter
XM_017011103.2:c.3556G>T	XP_016866592.1:p.Glu1186Ter
XM_017011104.1:c.3526G>T	XP_016866593.1:p.Glu1176Ter
XM_017011105.2:c.3496G>T	XP_016866594.1:p.Glu1166Ter
XM_017011106.2:c.3367G>T	XP_016866595.1:p.Glu1123Ter
XM_017011107.2:c.3346G>T	XP_016866596.1:p.Glu1116Ter
XR_002956289.1:n.3738G>T
NM_001363725.2:c.1195G>T	NP_001350654.1:p.Glu399Ter
NM_001371656.1:c.3574G>T	NP_001358585.1:p.Glu1192Ter
NM_001374820.1:c.3574G>T	NP_001361749.1:p.Glu1192Ter
NM_001374828.1:c.3694G>T MANE Select	NP_001361757.1:p.Glu1232Ter
NM_017519.3:c.3535G>T	NP_059989.3:p.Glu1179Ter