Canonical Allele Identifier: CA366228420

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231267
• gnomAD v4: 6-157181158-G-A
• MyVariant Identifiers: chr6:g.157502292G>A (hg19) ; chr6:g.157181158G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3535G>A	ENSP00000055163.8:p.Glu1179Lys
ENST00000414678.8:c.3604G>A	ENSP00000412835.3:p.Glu1202Lys
ENST00000637015.2:c.3823G>A	ENSP00000489729.2:p.Glu1275Lys
ENST00000319584.11:c.1708G>A	ENSP00000313006.7:p.Glu570Lys
ENST00000346085.10:c.3574G>A	ENSP00000344546.5:p.Glu1192Lys
ENST00000350026.10:c.3286G>A	ENSP00000055163.7:p.Glu1096Lys
ENST00000414678.7:c.1852G>A	ENSP00000412835.2:p.Glu618Lys
ENST00000635849.1:c.1015G>A	ENSP00000490948.1:p.Glu339Lys
ENST00000635957.1:c.649G>A	ENSP00000490385.1:p.Glu217Lys
ENST00000636930.2:c.3694G>A MANE Select	ENSP00000490491.2:p.Glu1232Lys
ENST00000636940.1:n.1691G>A
ENST00000637015.1:c.1062G>A
ENST00000637568.1:c.976G>A
ENST00000637741.1:n.360G>A
ENST00000637810.1:c.1036G>A	ENSP00000489636.1:p.Glu346Lys
ENST00000637904.1:c.1195G>A	ENSP00000490550.1:p.Glu399Lys
ENST00000647938.1:c.3325G>A	ENSP00000498155.1:p.Glu1109Lys
ENST00000319584.10:c.1711G>A	ENSP00000313006.6:p.Glu571Lys
ENST00000346085.9:c.3325G>A	ENSP00000344546.4:p.Glu1109Lys
ENST00000350026.9:c.3286G>A	ENSP00000055163.7:p.Glu1096Lys
ENST00000400790.3:c.487G>A	ENSP00000383596.3:p.Glu163Lys
ENST00000414678.6:c.1852G>A	ENSP00000412835.2:p.Glu618Lys
ENST00000478761.3:c.896G>A
NM_017519.2:c.3286G>A	NP_059989.2:p.Glu1096Lys
NM_020732.3:c.3325G>A	NP_065783.3:p.Glu1109Lys
XM_005267069.3:c.3445G>A	XP_005267126.2:p.Glu1149Lys
XM_011535984.1:c.2524G>A	XP_011534286.1:p.Glu842Lys
XM_011535985.1:c.2344G>A	XP_011534287.1:p.Glu782Lys
XM_011535986.1:c.2104G>A	XP_011534288.1:p.Glu702Lys
XM_011535987.1:c.1723G>A	XP_011534289.1:p.Glu575Lys
XM_011535988.1:c.586G>A	XP_011534290.1:p.Glu196Lys
NM_001346813.1:c.3445G>A	NP_001333742.1:p.Glu1149Lys
NM_001363725.1:c.1195G>A	NP_001350654.1:p.Glu399Lys
XM_011535984.2:c.3655G>A	XP_011534286.2:p.Glu1219Lys
XM_011535988.3:c.586G>A	XP_011534290.1:p.Glu196Lys
XM_017011103.2:c.3556G>A	XP_016866592.1:p.Glu1186Lys
XM_017011104.1:c.3526G>A	XP_016866593.1:p.Glu1176Lys
XM_017011105.2:c.3496G>A	XP_016866594.1:p.Glu1166Lys
XM_017011106.2:c.3367G>A	XP_016866595.1:p.Glu1123Lys
XM_017011107.2:c.3346G>A	XP_016866596.1:p.Glu1116Lys
XR_002956289.1:n.3738G>A
NM_001363725.2:c.1195G>A	NP_001350654.1:p.Glu399Lys
NM_001371656.1:c.3574G>A	NP_001358585.1:p.Glu1192Lys
NM_001374820.1:c.3574G>A	NP_001361749.1:p.Glu1192Lys
NM_001374828.1:c.3694G>A MANE Select	NP_001361757.1:p.Glu1232Lys
NM_017519.3:c.3535G>A	NP_059989.3:p.Glu1179Lys