Canonical Allele Identifier: CA366227845

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317222
• MyVariant Identifiers: chr6:g.157502210A>T (hg19) ; chr6:g.157181076A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3453A>T	ENSP00000055163.8:p.Glu1151Asp
ENST00000414678.8:c.3522A>T	ENSP00000412835.3:p.Glu1174Asp
ENST00000637015.2:c.3741A>T	ENSP00000489729.2:p.Glu1247Asp
ENST00000319584.11:c.1626A>T	ENSP00000313006.7:p.Glu542Asp
ENST00000346085.10:c.3492A>T	ENSP00000344546.5:p.Glu1164Asp
ENST00000350026.10:c.3204A>T	ENSP00000055163.7:p.Glu1068Asp
ENST00000414678.7:c.1770A>T	ENSP00000412835.2:p.Glu590Asp
ENST00000635849.1:c.933A>T	ENSP00000490948.1:p.Glu311Asp
ENST00000635957.1:c.567A>T	ENSP00000490385.1:p.Glu189Asp
ENST00000636930.2:c.3612A>T MANE Select	ENSP00000490491.2:p.Glu1204Asp
ENST00000636940.1:n.1609A>T
ENST00000637015.1:c.980A>T
ENST00000637568.1:c.894A>T
ENST00000637741.1:n.278A>T
ENST00000637810.1:c.954A>T	ENSP00000489636.1:p.Glu318Asp
ENST00000637904.1:c.1113A>T	ENSP00000490550.1:p.Glu371Asp
ENST00000647938.1:c.3243A>T	ENSP00000498155.1:p.Glu1081Asp
ENST00000319584.10:c.1629A>T	ENSP00000313006.6:p.Glu543Asp
ENST00000346085.9:c.3243A>T	ENSP00000344546.4:p.Glu1081Asp
ENST00000350026.9:c.3204A>T	ENSP00000055163.7:p.Glu1068Asp
ENST00000400790.3:c.405A>T	ENSP00000383596.3:p.Glu135Asp
ENST00000414678.6:c.1770A>T	ENSP00000412835.2:p.Glu590Asp
ENST00000478761.3:c.814A>T
NM_017519.2:c.3204A>T	NP_059989.2:p.Glu1068Asp
NM_020732.3:c.3243A>T	NP_065783.3:p.Glu1081Asp
XM_005267069.3:c.3363A>T	XP_005267126.2:p.Glu1121Asp
XM_011535984.1:c.2442A>T	XP_011534286.1:p.Glu814Asp
XM_011535985.1:c.2262A>T	XP_011534287.1:p.Glu754Asp
XM_011535986.1:c.2022A>T	XP_011534288.1:p.Glu674Asp
XM_011535987.1:c.1641A>T	XP_011534289.1:p.Glu547Asp
XM_011535988.1:c.504A>T	XP_011534290.1:p.Glu168Asp
NM_001346813.1:c.3363A>T	NP_001333742.1:p.Glu1121Asp
NM_001363725.1:c.1113A>T	NP_001350654.1:p.Glu371Asp
XM_011535984.2:c.3573A>T	XP_011534286.2:p.Glu1191Asp
XM_011535988.3:c.504A>T	XP_011534290.1:p.Glu168Asp
XM_017011103.2:c.3474A>T	XP_016866592.1:p.Glu1158Asp
XM_017011104.1:c.3444A>T	XP_016866593.1:p.Glu1148Asp
XM_017011105.2:c.3414A>T	XP_016866594.1:p.Glu1138Asp
XM_017011106.2:c.3285A>T	XP_016866595.1:p.Glu1095Asp
XM_017011107.2:c.3264A>T	XP_016866596.1:p.Glu1088Asp
XR_002956289.1:n.3656A>T
NM_001363725.2:c.1113A>T	NP_001350654.1:p.Glu371Asp
NM_001371656.1:c.3492A>T	NP_001358585.1:p.Glu1164Asp
NM_001374820.1:c.3492A>T	NP_001361749.1:p.Glu1164Asp
NM_001374828.1:c.3612A>T MANE Select	NP_001361757.1:p.Glu1204Asp
NM_017519.3:c.3453A>T	NP_059989.3:p.Glu1151Asp