Canonical Allele Identifier: CA366227838

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317219
• MyVariant Identifiers: chr6:g.157502209A>G (hg19) ; chr6:g.157181075A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181075A>G , CM000668.2:g.157181075A>G	GRCh38
NC_000006.11:g.157502209A>G , CM000668.1:g.157502209A>G	GRCh37
NC_000006.10:g.157543901A>G	NCBI36
NG_032093.1:g.408146A>G
NG_032093.2:g.408146A>G
NG_066624.1:g.410050A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3452A>G	ENSP00000055163.8:p.Glu1151Gly
ENST00000414678.8:c.3521A>G	ENSP00000412835.3:p.Glu1174Gly
ENST00000637015.2:c.3740A>G	ENSP00000489729.2:p.Glu1247Gly
ENST00000319584.11:c.1625A>G	ENSP00000313006.7:p.Glu542Gly
ENST00000346085.10:c.3491A>G	ENSP00000344546.5:p.Glu1164Gly
ENST00000350026.10:c.3203A>G	ENSP00000055163.7:p.Glu1068Gly
ENST00000414678.7:c.1769A>G	ENSP00000412835.2:p.Glu590Gly
ENST00000635849.1:c.932A>G	ENSP00000490948.1:p.Glu311Gly
ENST00000635957.1:c.566A>G	ENSP00000490385.1:p.Glu189Gly
ENST00000636930.2:c.3611A>G MANE Select	ENSP00000490491.2:p.Glu1204Gly
ENST00000636940.1:n.1608A>G
ENST00000637015.1:c.979A>G
ENST00000637568.1:c.893A>G
ENST00000637741.1:n.277A>G
ENST00000637810.1:c.953A>G	ENSP00000489636.1:p.Glu318Gly
ENST00000637904.1:c.1112A>G	ENSP00000490550.1:p.Glu371Gly
ENST00000647938.1:c.3242A>G	ENSP00000498155.1:p.Glu1081Gly
ENST00000319584.10:c.1628A>G	ENSP00000313006.6:p.Glu543Gly
ENST00000346085.9:c.3242A>G	ENSP00000344546.4:p.Glu1081Gly
ENST00000350026.9:c.3203A>G	ENSP00000055163.7:p.Glu1068Gly
ENST00000400790.3:c.404A>G	ENSP00000383596.3:p.Glu135Gly
ENST00000414678.6:c.1769A>G	ENSP00000412835.2:p.Glu590Gly
ENST00000478761.3:c.813A>G
NM_017519.2:c.3203A>G	NP_059989.2:p.Glu1068Gly
NM_020732.3:c.3242A>G	NP_065783.3:p.Glu1081Gly
XM_005267069.3:c.3362A>G	XP_005267126.2:p.Glu1121Gly
XM_011535984.1:c.2441A>G	XP_011534286.1:p.Glu814Gly
XM_011535985.1:c.2261A>G	XP_011534287.1:p.Glu754Gly
XM_011535986.1:c.2021A>G	XP_011534288.1:p.Glu674Gly
XM_011535987.1:c.1640A>G	XP_011534289.1:p.Glu547Gly
XM_011535988.1:c.503A>G	XP_011534290.1:p.Glu168Gly
NM_001346813.1:c.3362A>G	NP_001333742.1:p.Glu1121Gly
NM_001363725.1:c.1112A>G	NP_001350654.1:p.Glu371Gly
XM_011535984.2:c.3572A>G	XP_011534286.2:p.Glu1191Gly
XM_011535988.3:c.503A>G	XP_011534290.1:p.Glu168Gly
XM_017011103.2:c.3473A>G	XP_016866592.1:p.Glu1158Gly
XM_017011104.1:c.3443A>G	XP_016866593.1:p.Glu1148Gly
XM_017011105.2:c.3413A>G	XP_016866594.1:p.Glu1138Gly
XM_017011106.2:c.3284A>G	XP_016866595.1:p.Glu1095Gly
XM_017011107.2:c.3263A>G	XP_016866596.1:p.Glu1088Gly
XR_002956289.1:n.3655A>G
NM_001363725.2:c.1112A>G	NP_001350654.1:p.Glu371Gly
NM_001371656.1:c.3491A>G	NP_001358585.1:p.Glu1164Gly
NM_001374820.1:c.3491A>G	NP_001361749.1:p.Glu1164Gly
NM_001374828.1:c.3611A>G MANE Select	NP_001361757.1:p.Glu1204Gly
NM_017519.3:c.3452A>G	NP_059989.3:p.Glu1151Gly