Canonical Allele Identifier: CA366227842

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3452A>T	ENSP00000055163.8:p.Glu1151Val
ENST00000414678.8:c.3521A>T	ENSP00000412835.3:p.Glu1174Val
ENST00000637015.2:c.3740A>T	ENSP00000489729.2:p.Glu1247Val
ENST00000319584.11:c.1625A>T	ENSP00000313006.7:p.Glu542Val
ENST00000346085.10:c.3491A>T	ENSP00000344546.5:p.Glu1164Val
ENST00000350026.10:c.3203A>T	ENSP00000055163.7:p.Glu1068Val
ENST00000414678.7:c.1769A>T	ENSP00000412835.2:p.Glu590Val
ENST00000635849.1:c.932A>T	ENSP00000490948.1:p.Glu311Val
ENST00000635957.1:c.566A>T	ENSP00000490385.1:p.Glu189Val
ENST00000636930.2:c.3611A>T MANE Select	ENSP00000490491.2:p.Glu1204Val
ENST00000636940.1:n.1608A>T
ENST00000637015.1:c.979A>T
ENST00000637568.1:c.893A>T
ENST00000637741.1:n.277A>T
ENST00000637810.1:c.953A>T	ENSP00000489636.1:p.Glu318Val
ENST00000637904.1:c.1112A>T	ENSP00000490550.1:p.Glu371Val
ENST00000647938.1:c.3242A>T	ENSP00000498155.1:p.Glu1081Val
ENST00000319584.10:c.1628A>T	ENSP00000313006.6:p.Glu543Val
ENST00000346085.9:c.3242A>T	ENSP00000344546.4:p.Glu1081Val
ENST00000350026.9:c.3203A>T	ENSP00000055163.7:p.Glu1068Val
ENST00000400790.3:c.404A>T	ENSP00000383596.3:p.Glu135Val
ENST00000414678.6:c.1769A>T	ENSP00000412835.2:p.Glu590Val
ENST00000478761.3:c.813A>T
NM_017519.2:c.3203A>T	NP_059989.2:p.Glu1068Val
NM_020732.3:c.3242A>T	NP_065783.3:p.Glu1081Val
XM_005267069.3:c.3362A>T	XP_005267126.2:p.Glu1121Val
XM_011535984.1:c.2441A>T	XP_011534286.1:p.Glu814Val
XM_011535985.1:c.2261A>T	XP_011534287.1:p.Glu754Val
XM_011535986.1:c.2021A>T	XP_011534288.1:p.Glu674Val
XM_011535987.1:c.1640A>T	XP_011534289.1:p.Glu547Val
XM_011535988.1:c.503A>T	XP_011534290.1:p.Glu168Val
NM_001346813.1:c.3362A>T	NP_001333742.1:p.Glu1121Val
NM_001363725.1:c.1112A>T	NP_001350654.1:p.Glu371Val
XM_011535984.2:c.3572A>T	XP_011534286.2:p.Glu1191Val
XM_011535988.3:c.503A>T	XP_011534290.1:p.Glu168Val
XM_017011103.2:c.3473A>T	XP_016866592.1:p.Glu1158Val
XM_017011104.1:c.3443A>T	XP_016866593.1:p.Glu1148Val
XM_017011105.2:c.3413A>T	XP_016866594.1:p.Glu1138Val
XM_017011106.2:c.3284A>T	XP_016866595.1:p.Glu1095Val
XM_017011107.2:c.3263A>T	XP_016866596.1:p.Glu1088Val
XR_002956289.1:n.3655A>T
NM_001363725.2:c.1112A>T	NP_001350654.1:p.Glu371Val
NM_001371656.1:c.3491A>T	NP_001358585.1:p.Glu1164Val
NM_001374820.1:c.3491A>T	NP_001361749.1:p.Glu1164Val
NM_001374828.1:c.3611A>T MANE Select	NP_001361757.1:p.Glu1204Val
NM_017519.3:c.3452A>T	NP_059989.3:p.Glu1151Val