Canonical Allele Identifier: CA366227828

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554231225
• MyVariant Identifiers: chr6:g.157502208G>T (hg19) ; chr6:g.157181074G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181074G>T , CM000668.2:g.157181074G>T	GRCh38
NC_000006.11:g.157502208G>T , CM000668.1:g.157502208G>T	GRCh37
NC_000006.10:g.157543900G>T	NCBI36
NG_032093.1:g.408145G>T
NG_032093.2:g.408145G>T
NG_066624.1:g.410049G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3451G>T	ENSP00000055163.8:p.Glu1151Ter
ENST00000414678.8:c.3520G>T	ENSP00000412835.3:p.Glu1174Ter
ENST00000637015.2:c.3739G>T	ENSP00000489729.2:p.Glu1247Ter
ENST00000319584.11:c.1624G>T	ENSP00000313006.7:p.Glu542Ter
ENST00000346085.10:c.3490G>T	ENSP00000344546.5:p.Glu1164Ter
ENST00000350026.10:c.3202G>T	ENSP00000055163.7:p.Glu1068Ter
ENST00000414678.7:c.1768G>T	ENSP00000412835.2:p.Glu590Ter
ENST00000635849.1:c.931G>T	ENSP00000490948.1:p.Glu311Ter
ENST00000635957.1:c.565G>T	ENSP00000490385.1:p.Glu189Ter
ENST00000636930.2:c.3610G>T MANE Select	ENSP00000490491.2:p.Glu1204Ter
ENST00000636940.1:n.1607G>T
ENST00000637015.1:c.978G>T
ENST00000637568.1:c.892G>T
ENST00000637741.1:n.276G>T
ENST00000637810.1:c.952G>T	ENSP00000489636.1:p.Glu318Ter
ENST00000637904.1:c.1111G>T	ENSP00000490550.1:p.Glu371Ter
ENST00000647938.1:c.3241G>T	ENSP00000498155.1:p.Glu1081Ter
ENST00000319584.10:c.1627G>T	ENSP00000313006.6:p.Glu543Ter
ENST00000346085.9:c.3241G>T	ENSP00000344546.4:p.Glu1081Ter
ENST00000350026.9:c.3202G>T	ENSP00000055163.7:p.Glu1068Ter
ENST00000400790.3:c.403G>T	ENSP00000383596.3:p.Glu135Ter
ENST00000414678.6:c.1768G>T	ENSP00000412835.2:p.Glu590Ter
ENST00000478761.3:c.812G>T
NM_017519.2:c.3202G>T	NP_059989.2:p.Glu1068Ter
NM_020732.3:c.3241G>T	NP_065783.3:p.Glu1081Ter
XM_005267069.3:c.3361G>T	XP_005267126.2:p.Glu1121Ter
XM_011535984.1:c.2440G>T	XP_011534286.1:p.Glu814Ter
XM_011535985.1:c.2260G>T	XP_011534287.1:p.Glu754Ter
XM_011535986.1:c.2020G>T	XP_011534288.1:p.Glu674Ter
XM_011535987.1:c.1639G>T	XP_011534289.1:p.Glu547Ter
XM_011535988.1:c.502G>T	XP_011534290.1:p.Glu168Ter
NM_001346813.1:c.3361G>T	NP_001333742.1:p.Glu1121Ter
NM_001363725.1:c.1111G>T	NP_001350654.1:p.Glu371Ter
XM_011535984.2:c.3571G>T	XP_011534286.2:p.Glu1191Ter
XM_011535988.3:c.502G>T	XP_011534290.1:p.Glu168Ter
XM_017011103.2:c.3472G>T	XP_016866592.1:p.Glu1158Ter
XM_017011104.1:c.3442G>T	XP_016866593.1:p.Glu1148Ter
XM_017011105.2:c.3412G>T	XP_016866594.1:p.Glu1138Ter
XM_017011106.2:c.3283G>T	XP_016866595.1:p.Glu1095Ter
XM_017011107.2:c.3262G>T	XP_016866596.1:p.Glu1088Ter
XR_002956289.1:n.3654G>T
NM_001363725.2:c.1111G>T	NP_001350654.1:p.Glu371Ter
NM_001371656.1:c.3490G>T	NP_001358585.1:p.Glu1164Ter
NM_001374820.1:c.3490G>T	NP_001361749.1:p.Glu1164Ter
NM_001374828.1:c.3610G>T MANE Select	NP_001361757.1:p.Glu1204Ter
NM_017519.3:c.3451G>T	NP_059989.3:p.Glu1151Ter