Canonical Allele Identifier: CA16618267

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 420932
• ClinVar RCV Id: RCV000486528
• dbSNP Id: rs1064794799
• MyVariant Identifiers: chr6:g.157528399G>A (hg19) ; chr6:g.157207265G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.6334G>A	ENSP00000055163.8:p.Glu2112Lys
ENST00000414678.8:c.6403G>A	ENSP00000412835.3:p.Glu2135Lys
ENST00000637015.2:c.6622G>A	ENSP00000489729.2:p.Glu2208Lys
ENST00000346085.10:c.6373G>A	ENSP00000344546.5:p.Glu2125Lys
ENST00000350026.10:c.6085G>A	ENSP00000055163.7:p.Glu2029Lys
ENST00000414678.7:c.4651G>A	ENSP00000412835.2:p.Glu1551Lys
ENST00000635849.1:c.3814G>A	ENSP00000490948.1:p.Glu1272Lys
ENST00000635928.1:c.649G>A	ENSP00000489717.1:p.Glu217Lys
ENST00000635957.1:c.3445G>A	ENSP00000490385.1:p.Glu1149Lys
ENST00000636227.1:n.4956G>A
ENST00000636254.1:n.2413G>A
ENST00000636930.2:c.6493G>A MANE Select	ENSP00000490491.2:p.Glu2165Lys
ENST00000636940.1:n.4490G>A
ENST00000637015.1:c.3861G>A
ENST00000637568.1:c.3775G>A
ENST00000637741.1:n.3159G>A
ENST00000637810.1:c.3835G>A	ENSP00000489636.1:p.Glu1279Lys
ENST00000637904.1:c.3994G>A	ENSP00000490550.1:p.Glu1332Lys
ENST00000637933.1:n.3608G>A
ENST00000647938.1:c.6124G>A	ENSP00000498155.1:p.Glu2042Lys
ENST00000346085.9:c.6124G>A	ENSP00000344546.4:p.Glu2042Lys
ENST00000350026.9:c.6085G>A	ENSP00000055163.7:p.Glu2029Lys
ENST00000414678.6:c.4651G>A	ENSP00000412835.2:p.Glu1551Lys
NM_017519.2:c.6085G>A	NP_059989.2:p.Glu2029Lys
NM_020732.3:c.6124G>A	NP_065783.3:p.Glu2042Lys
XM_005267069.3:c.6244G>A	XP_005267126.2:p.Glu2082Lys
XM_011535984.1:c.5323G>A	XP_011534286.1:p.Glu1775Lys
XM_011535985.1:c.5143G>A	XP_011534287.1:p.Glu1715Lys
XM_011535986.1:c.4903G>A	XP_011534288.1:p.Glu1635Lys
XM_011535987.1:c.4522G>A	XP_011534289.1:p.Glu1508Lys
XM_011535988.1:c.3385G>A	XP_011534290.1:p.Glu1129Lys
NM_001346813.1:c.6244G>A	NP_001333742.1:p.Glu2082Lys
NM_001363725.1:c.3994G>A	NP_001350654.1:p.Glu1332Lys
XM_011535984.2:c.6454G>A	XP_011534286.2:p.Glu2152Lys
XM_011535988.3:c.3385G>A	XP_011534290.1:p.Glu1129Lys
XM_017011103.2:c.6355G>A	XP_016866592.1:p.Glu2119Lys
XM_017011104.1:c.6325G>A	XP_016866593.1:p.Glu2109Lys
XM_017011105.2:c.6295G>A	XP_016866594.1:p.Glu2099Lys
XM_017011106.2:c.6166G>A	XP_016866595.1:p.Glu2056Lys
XM_017011107.2:c.6145G>A	XP_016866596.1:p.Glu2049Lys
XR_002956289.1:n.6440G>A
NM_001363725.2:c.3994G>A	NP_001350654.1:p.Glu1332Lys
NM_001371656.1:c.6373G>A	NP_001358585.1:p.Glu2125Lys
NM_001374820.1:c.6373G>A	NP_001361749.1:p.Glu2125Lys
NM_001374828.1:c.6493G>A MANE Select	NP_001361757.1:p.Glu2165Lys
NM_017519.3:c.6334G>A	NP_059989.3:p.Glu2112Lys