Canonical Allele Identifier: CA366248401

Gene: ARID1B

Linked Data

• dbSNP Id: rs1064794799
• MyVariant Identifiers: chr6:g.157528399G>T (hg19) ; chr6:g.157207265G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207265G>T , CM000668.2:g.157207265G>T	GRCh38
NC_000006.11:g.157528399G>T , CM000668.1:g.157528399G>T	GRCh37
NC_000006.10:g.157570091G>T	NCBI36
NG_032093.1:g.434336G>T
NG_032093.2:g.434336G>T
NG_066624.1:g.436240G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.6334G>T	ENSP00000055163.8:p.Glu2112Ter
ENST00000414678.8:c.6403G>T	ENSP00000412835.3:p.Glu2135Ter
ENST00000637015.2:c.6622G>T	ENSP00000489729.2:p.Glu2208Ter
ENST00000346085.10:c.6373G>T	ENSP00000344546.5:p.Glu2125Ter
ENST00000350026.10:c.6085G>T	ENSP00000055163.7:p.Glu2029Ter
ENST00000414678.7:c.4651G>T	ENSP00000412835.2:p.Glu1551Ter
ENST00000635849.1:c.3814G>T	ENSP00000490948.1:p.Glu1272Ter
ENST00000635928.1:c.649G>T	ENSP00000489717.1:p.Glu217Ter
ENST00000635957.1:c.3445G>T	ENSP00000490385.1:p.Glu1149Ter
ENST00000636227.1:n.4956G>T
ENST00000636254.1:n.2413G>T
ENST00000636930.2:c.6493G>T MANE Select	ENSP00000490491.2:p.Glu2165Ter
ENST00000636940.1:n.4490G>T
ENST00000637015.1:c.3861G>T
ENST00000637568.1:c.3775G>T
ENST00000637741.1:n.3159G>T
ENST00000637810.1:c.3835G>T	ENSP00000489636.1:p.Glu1279Ter
ENST00000637904.1:c.3994G>T	ENSP00000490550.1:p.Glu1332Ter
ENST00000637933.1:n.3608G>T
ENST00000647938.1:c.6124G>T	ENSP00000498155.1:p.Glu2042Ter
ENST00000346085.9:c.6124G>T	ENSP00000344546.4:p.Glu2042Ter
ENST00000350026.9:c.6085G>T	ENSP00000055163.7:p.Glu2029Ter
ENST00000414678.6:c.4651G>T	ENSP00000412835.2:p.Glu1551Ter
NM_017519.2:c.6085G>T	NP_059989.2:p.Glu2029Ter
NM_020732.3:c.6124G>T	NP_065783.3:p.Glu2042Ter
XM_005267069.3:c.6244G>T	XP_005267126.2:p.Glu2082Ter
XM_011535984.1:c.5323G>T	XP_011534286.1:p.Glu1775Ter
XM_011535985.1:c.5143G>T	XP_011534287.1:p.Glu1715Ter
XM_011535986.1:c.4903G>T	XP_011534288.1:p.Glu1635Ter
XM_011535987.1:c.4522G>T	XP_011534289.1:p.Glu1508Ter
XM_011535988.1:c.3385G>T	XP_011534290.1:p.Glu1129Ter
NM_001346813.1:c.6244G>T	NP_001333742.1:p.Glu2082Ter
NM_001363725.1:c.3994G>T	NP_001350654.1:p.Glu1332Ter
XM_011535984.2:c.6454G>T	XP_011534286.2:p.Glu2152Ter
XM_011535988.3:c.3385G>T	XP_011534290.1:p.Glu1129Ter
XM_017011103.2:c.6355G>T	XP_016866592.1:p.Glu2119Ter
XM_017011104.1:c.6325G>T	XP_016866593.1:p.Glu2109Ter
XM_017011105.2:c.6295G>T	XP_016866594.1:p.Glu2099Ter
XM_017011106.2:c.6166G>T	XP_016866595.1:p.Glu2056Ter
XM_017011107.2:c.6145G>T	XP_016866596.1:p.Glu2049Ter
XR_002956289.1:n.6440G>T
NM_001363725.2:c.3994G>T	NP_001350654.1:p.Glu1332Ter
NM_001371656.1:c.6373G>T	NP_001358585.1:p.Glu2125Ter
NM_001374820.1:c.6373G>T	NP_001361749.1:p.Glu2125Ter
NM_001374828.1:c.6493G>T MANE Select	NP_001361757.1:p.Glu2165Ter
NM_017519.3:c.6334G>T	NP_059989.3:p.Glu2112Ter