Canonical Allele Identifier: CA366242701

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376167
• MyVariant Identifiers: chr6:g.157522487G>A (hg19) ; chr6:g.157201353G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201353G>A , CM000668.2:g.157201353G>A	GRCh38
NC_000006.11:g.157522487G>A , CM000668.1:g.157522487G>A	GRCh37
NC_000006.10:g.157564179G>A	NCBI36
NG_032093.1:g.428424G>A
NG_032093.2:g.428424G>A
NG_066624.1:g.430328G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4969G>A	ENSP00000055163.8:p.Val1657Ile
ENST00000414678.8:c.5038G>A	ENSP00000412835.3:p.Val1680Ile
ENST00000637015.2:c.5257G>A	ENSP00000489729.2:p.Val1753Ile
ENST00000346085.10:c.5008G>A	ENSP00000344546.5:p.Val1670Ile
ENST00000350026.10:c.4720G>A	ENSP00000055163.7:p.Val1574Ile
ENST00000414678.7:c.3286G>A	ENSP00000412835.2:p.Val1096Ile
ENST00000635849.1:c.2449G>A	ENSP00000490948.1:p.Val817Ile
ENST00000635957.1:c.2080G>A	ENSP00000490385.1:p.Val694Ile
ENST00000636227.1:n.3591G>A
ENST00000636254.1:n.1048G>A
ENST00000636930.2:c.5128G>A MANE Select	ENSP00000490491.2:p.Val1710Ile
ENST00000636940.1:n.3125G>A
ENST00000637015.1:c.2496G>A
ENST00000637568.1:c.2410G>A
ENST00000637741.1:n.1794G>A
ENST00000637810.1:c.2470G>A	ENSP00000489636.1:p.Val824Ile
ENST00000637904.1:c.2629G>A	ENSP00000490550.1:p.Val877Ile
ENST00000647938.1:c.4759G>A	ENSP00000498155.1:p.Val1587Ile
ENST00000346085.9:c.4759G>A	ENSP00000344546.4:p.Val1587Ile
ENST00000350026.9:c.4720G>A	ENSP00000055163.7:p.Val1574Ile
ENST00000414678.6:c.3286G>A	ENSP00000412835.2:p.Val1096Ile
NM_017519.2:c.4720G>A	NP_059989.2:p.Val1574Ile
NM_020732.3:c.4759G>A	NP_065783.3:p.Val1587Ile
XM_005267069.3:c.4879G>A	XP_005267126.2:p.Val1627Ile
XM_011535984.1:c.3958G>A	XP_011534286.1:p.Val1320Ile
XM_011535985.1:c.3778G>A	XP_011534287.1:p.Val1260Ile
XM_011535986.1:c.3538G>A	XP_011534288.1:p.Val1180Ile
XM_011535987.1:c.3157G>A	XP_011534289.1:p.Val1053Ile
XM_011535988.1:c.2020G>A	XP_011534290.1:p.Val674Ile
NM_001346813.1:c.4879G>A	NP_001333742.1:p.Val1627Ile
NM_001363725.1:c.2629G>A	NP_001350654.1:p.Val877Ile
XM_011535984.2:c.5089G>A	XP_011534286.2:p.Val1697Ile
XM_011535988.3:c.2020G>A	XP_011534290.1:p.Val674Ile
XM_017011103.2:c.4990G>A	XP_016866592.1:p.Val1664Ile
XM_017011104.1:c.4960G>A	XP_016866593.1:p.Val1654Ile
XM_017011105.2:c.4930G>A	XP_016866594.1:p.Val1644Ile
XM_017011106.2:c.4801G>A	XP_016866595.1:p.Val1601Ile
XM_017011107.2:c.4780G>A	XP_016866596.1:p.Val1594Ile
XR_002956289.1:n.5075G>A
NM_001363725.2:c.2629G>A	NP_001350654.1:p.Val877Ile
NM_001371656.1:c.5008G>A	NP_001358585.1:p.Val1670Ile
NM_001374820.1:c.5008G>A	NP_001361749.1:p.Val1670Ile
NM_001374828.1:c.5128G>A MANE Select	NP_001361757.1:p.Val1710Ile
NM_017519.3:c.4969G>A	NP_059989.3:p.Val1657Ile