Canonical Allele Identifier: CA452780774

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502210A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181076A>G , CM000668.2:g.157181076A>G	GRCh38
NC_000006.11:g.157502210A>G , CM000668.1:g.157502210A>G	GRCh37
NC_000006.10:g.157543902A>G	NCBI36
NG_032093.1:g.408147A>G
NG_032093.2:g.408147A>G
NG_066624.1:g.410051A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3453A>G	ENSP00000055163.8:p.Glu1151=
ENST00000414678.8:c.3522A>G	ENSP00000412835.3:p.Glu1174=
ENST00000637015.2:c.3741A>G	ENSP00000489729.2:p.Glu1247=
ENST00000319584.11:c.1626A>G	ENSP00000313006.7:p.Glu542=
ENST00000346085.10:c.3492A>G	ENSP00000344546.5:p.Glu1164=
ENST00000350026.10:c.3204A>G	ENSP00000055163.7:p.Glu1068=
ENST00000414678.7:c.1770A>G	ENSP00000412835.2:p.Glu590=
ENST00000635849.1:c.933A>G	ENSP00000490948.1:p.Glu311=
ENST00000635957.1:c.567A>G	ENSP00000490385.1:p.Glu189=
ENST00000636930.2:c.3612A>G MANE Select	ENSP00000490491.2:p.Glu1204=
ENST00000636940.1:n.1609A>G
ENST00000637015.1:c.980A>G
ENST00000637568.1:c.894A>G
ENST00000637741.1:n.278A>G
ENST00000637810.1:c.954A>G	ENSP00000489636.1:p.Glu318=
ENST00000637904.1:c.1113A>G	ENSP00000490550.1:p.Glu371=
ENST00000647938.1:c.3243A>G	ENSP00000498155.1:p.Glu1081=
ENST00000319584.10:c.1629A>G	ENSP00000313006.6:p.Glu543=
ENST00000346085.9:c.3243A>G	ENSP00000344546.4:p.Glu1081=
ENST00000350026.9:c.3204A>G	ENSP00000055163.7:p.Glu1068=
ENST00000400790.3:c.405A>G	ENSP00000383596.3:p.Glu135=
ENST00000414678.6:c.1770A>G	ENSP00000412835.2:p.Glu590=
ENST00000478761.3:c.814A>G
NM_017519.2:c.3204A>G	NP_059989.2:p.Glu1068=
NM_020732.3:c.3243A>G	NP_065783.3:p.Glu1081=
XM_005267069.3:c.3363A>G	XP_005267126.2:p.Glu1121=
XM_011535984.1:c.2442A>G	XP_011534286.1:p.Glu814=
XM_011535985.1:c.2262A>G	XP_011534287.1:p.Glu754=
XM_011535986.1:c.2022A>G	XP_011534288.1:p.Glu674=
XM_011535987.1:c.1641A>G	XP_011534289.1:p.Glu547=
XM_011535988.1:c.504A>G	XP_011534290.1:p.Glu168=
NM_001346813.1:c.3363A>G	NP_001333742.1:p.Glu1121=
NM_001363725.1:c.1113A>G	NP_001350654.1:p.Glu371=
XM_011535984.2:c.3573A>G	XP_011534286.2:p.Glu1191=
XM_011535988.3:c.504A>G	XP_011534290.1:p.Glu168=
XM_017011103.2:c.3474A>G	XP_016866592.1:p.Glu1158=
XM_017011104.1:c.3444A>G	XP_016866593.1:p.Glu1148=
XM_017011105.2:c.3414A>G	XP_016866594.1:p.Glu1138=
XM_017011106.2:c.3285A>G	XP_016866595.1:p.Glu1095=
XM_017011107.2:c.3264A>G	XP_016866596.1:p.Glu1088=
XR_002956289.1:n.3656A>G
NM_001363725.2:c.1113A>G	NP_001350654.1:p.Glu371=
NM_001371656.1:c.3492A>G	NP_001358585.1:p.Glu1164=
NM_001374820.1:c.3492A>G	NP_001361749.1:p.Glu1164=
NM_001374828.1:c.3612A>G MANE Select	NP_001361757.1:p.Glu1204=
NM_017519.3:c.3453A>G	NP_059989.3:p.Glu1151=