Canonical Allele Identifier: CA366242642

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376046
• MyVariant Identifiers: chr6:g.157522476T>A (hg19) ; chr6:g.157201342T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201342T>A , CM000668.2:g.157201342T>A	GRCh38
NC_000006.11:g.157522476T>A , CM000668.1:g.157522476T>A	GRCh37
NC_000006.10:g.157564168T>A	NCBI36
NG_032093.1:g.428413T>A
NG_032093.2:g.428413T>A
NG_066624.1:g.430317T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4958T>A	ENSP00000055163.8:p.Val1653Asp
ENST00000414678.8:c.5027T>A	ENSP00000412835.3:p.Val1676Asp
ENST00000637015.2:c.5246T>A	ENSP00000489729.2:p.Val1749Asp
ENST00000346085.10:c.4997T>A	ENSP00000344546.5:p.Val1666Asp
ENST00000350026.10:c.4709T>A	ENSP00000055163.7:p.Val1570Asp
ENST00000414678.7:c.3275T>A	ENSP00000412835.2:p.Val1092Asp
ENST00000635849.1:c.2438T>A	ENSP00000490948.1:p.Val813Asp
ENST00000635957.1:c.2069T>A	ENSP00000490385.1:p.Val690Asp
ENST00000636227.1:n.3580T>A
ENST00000636254.1:n.1037T>A
ENST00000636930.2:c.5117T>A MANE Select	ENSP00000490491.2:p.Val1706Asp
ENST00000636940.1:n.3114T>A
ENST00000637015.1:c.2485T>A
ENST00000637568.1:c.2399T>A
ENST00000637741.1:n.1783T>A
ENST00000637810.1:c.2459T>A	ENSP00000489636.1:p.Val820Asp
ENST00000637904.1:c.2618T>A	ENSP00000490550.1:p.Val873Asp
ENST00000647938.1:c.4748T>A	ENSP00000498155.1:p.Val1583Asp
ENST00000346085.9:c.4748T>A	ENSP00000344546.4:p.Val1583Asp
ENST00000350026.9:c.4709T>A	ENSP00000055163.7:p.Val1570Asp
ENST00000414678.6:c.3275T>A	ENSP00000412835.2:p.Val1092Asp
NM_017519.2:c.4709T>A	NP_059989.2:p.Val1570Asp
NM_020732.3:c.4748T>A	NP_065783.3:p.Val1583Asp
XM_005267069.3:c.4868T>A	XP_005267126.2:p.Val1623Asp
XM_011535984.1:c.3947T>A	XP_011534286.1:p.Val1316Asp
XM_011535985.1:c.3767T>A	XP_011534287.1:p.Val1256Asp
XM_011535986.1:c.3527T>A	XP_011534288.1:p.Val1176Asp
XM_011535987.1:c.3146T>A	XP_011534289.1:p.Val1049Asp
XM_011535988.1:c.2009T>A	XP_011534290.1:p.Val670Asp
NM_001346813.1:c.4868T>A	NP_001333742.1:p.Val1623Asp
NM_001363725.1:c.2618T>A	NP_001350654.1:p.Val873Asp
XM_011535984.2:c.5078T>A	XP_011534286.2:p.Val1693Asp
XM_011535988.3:c.2009T>A	XP_011534290.1:p.Val670Asp
XM_017011103.2:c.4979T>A	XP_016866592.1:p.Val1660Asp
XM_017011104.1:c.4949T>A	XP_016866593.1:p.Val1650Asp
XM_017011105.2:c.4919T>A	XP_016866594.1:p.Val1640Asp
XM_017011106.2:c.4790T>A	XP_016866595.1:p.Val1597Asp
XM_017011107.2:c.4769T>A	XP_016866596.1:p.Val1590Asp
XR_002956289.1:n.5064T>A
NM_001363725.2:c.2618T>A	NP_001350654.1:p.Val873Asp
NM_001371656.1:c.4997T>A	NP_001358585.1:p.Val1666Asp
NM_001374820.1:c.4997T>A	NP_001361749.1:p.Val1666Asp
NM_001374828.1:c.5117T>A MANE Select	NP_001361757.1:p.Val1706Asp
NM_017519.3:c.4958T>A	NP_059989.3:p.Val1653Asp