Canonical Allele Identifier: CA452780802

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317490
• MyVariant Identifiers: chr6:g.157502249C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181115C>G , CM000668.2:g.157181115C>G	GRCh38
NC_000006.11:g.157502249C>G , CM000668.1:g.157502249C>G	GRCh37
NC_000006.10:g.157543941C>G	NCBI36
NG_032093.1:g.408186C>G
NG_032093.2:g.408186C>G
NG_066624.1:g.410090C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3492C>G	ENSP00000055163.8:p.Gly1164=
ENST00000414678.8:c.3561C>G	ENSP00000412835.3:p.Gly1187=
ENST00000637015.2:c.3780C>G	ENSP00000489729.2:p.Gly1260=
ENST00000319584.11:c.1665C>G	ENSP00000313006.7:p.Gly555=
ENST00000346085.10:c.3531C>G	ENSP00000344546.5:p.Gly1177=
ENST00000350026.10:c.3243C>G	ENSP00000055163.7:p.Gly1081=
ENST00000414678.7:c.1809C>G	ENSP00000412835.2:p.Gly603=
ENST00000635849.1:c.972C>G	ENSP00000490948.1:p.Gly324=
ENST00000635957.1:c.606C>G	ENSP00000490385.1:p.Gly202=
ENST00000636930.2:c.3651C>G MANE Select	ENSP00000490491.2:p.Gly1217=
ENST00000636940.1:n.1648C>G
ENST00000637015.1:c.1019C>G
ENST00000637568.1:c.933C>G
ENST00000637741.1:n.317C>G
ENST00000637810.1:c.993C>G	ENSP00000489636.1:p.Gly331=
ENST00000637904.1:c.1152C>G	ENSP00000490550.1:p.Gly384=
ENST00000647938.1:c.3282C>G	ENSP00000498155.1:p.Gly1094=
ENST00000319584.10:c.1668C>G	ENSP00000313006.6:p.Gly556=
ENST00000346085.9:c.3282C>G	ENSP00000344546.4:p.Gly1094=
ENST00000350026.9:c.3243C>G	ENSP00000055163.7:p.Gly1081=
ENST00000400790.3:c.444C>G	ENSP00000383596.3:p.Gly148=
ENST00000414678.6:c.1809C>G	ENSP00000412835.2:p.Gly603=
ENST00000478761.3:c.853C>G
NM_017519.2:c.3243C>G	NP_059989.2:p.Gly1081=
NM_020732.3:c.3282C>G	NP_065783.3:p.Gly1094=
XM_005267069.3:c.3402C>G	XP_005267126.2:p.Gly1134=
XM_011535984.1:c.2481C>G	XP_011534286.1:p.Gly827=
XM_011535985.1:c.2301C>G	XP_011534287.1:p.Gly767=
XM_011535986.1:c.2061C>G	XP_011534288.1:p.Gly687=
XM_011535987.1:c.1680C>G	XP_011534289.1:p.Gly560=
XM_011535988.1:c.543C>G	XP_011534290.1:p.Gly181=
NM_001346813.1:c.3402C>G	NP_001333742.1:p.Gly1134=
NM_001363725.1:c.1152C>G	NP_001350654.1:p.Gly384=
XM_011535984.2:c.3612C>G	XP_011534286.2:p.Gly1204=
XM_011535988.3:c.543C>G	XP_011534290.1:p.Gly181=
XM_017011103.2:c.3513C>G	XP_016866592.1:p.Gly1171=
XM_017011104.1:c.3483C>G	XP_016866593.1:p.Gly1161=
XM_017011105.2:c.3453C>G	XP_016866594.1:p.Gly1151=
XM_017011106.2:c.3324C>G	XP_016866595.1:p.Gly1108=
XM_017011107.2:c.3303C>G	XP_016866596.1:p.Gly1101=
XR_002956289.1:n.3695C>G
NM_001363725.2:c.1152C>G	NP_001350654.1:p.Gly384=
NM_001371656.1:c.3531C>G	NP_001358585.1:p.Gly1177=
NM_001374820.1:c.3531C>G	NP_001361749.1:p.Gly1177=
NM_001374828.1:c.3651C>G MANE Select	NP_001361757.1:p.Gly1217=
NM_017519.3:c.3492C>G	NP_059989.3:p.Gly1164=