Canonical Allele Identifier: CA366242646

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376046
• gnomAD v4: 6-157201342-T-G
• MyVariant Identifiers: chr6:g.157522476T>G (hg19) ; chr6:g.157201342T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4958T>G	ENSP00000055163.8:p.Val1653Gly
ENST00000414678.8:c.5027T>G	ENSP00000412835.3:p.Val1676Gly
ENST00000637015.2:c.5246T>G	ENSP00000489729.2:p.Val1749Gly
ENST00000346085.10:c.4997T>G	ENSP00000344546.5:p.Val1666Gly
ENST00000350026.10:c.4709T>G	ENSP00000055163.7:p.Val1570Gly
ENST00000414678.7:c.3275T>G	ENSP00000412835.2:p.Val1092Gly
ENST00000635849.1:c.2438T>G	ENSP00000490948.1:p.Val813Gly
ENST00000635957.1:c.2069T>G	ENSP00000490385.1:p.Val690Gly
ENST00000636227.1:n.3580T>G
ENST00000636254.1:n.1037T>G
ENST00000636930.2:c.5117T>G MANE Select	ENSP00000490491.2:p.Val1706Gly
ENST00000636940.1:n.3114T>G
ENST00000637015.1:c.2485T>G
ENST00000637568.1:c.2399T>G
ENST00000637741.1:n.1783T>G
ENST00000637810.1:c.2459T>G	ENSP00000489636.1:p.Val820Gly
ENST00000637904.1:c.2618T>G	ENSP00000490550.1:p.Val873Gly
ENST00000647938.1:c.4748T>G	ENSP00000498155.1:p.Val1583Gly
ENST00000346085.9:c.4748T>G	ENSP00000344546.4:p.Val1583Gly
ENST00000350026.9:c.4709T>G	ENSP00000055163.7:p.Val1570Gly
ENST00000414678.6:c.3275T>G	ENSP00000412835.2:p.Val1092Gly
NM_017519.2:c.4709T>G	NP_059989.2:p.Val1570Gly
NM_020732.3:c.4748T>G	NP_065783.3:p.Val1583Gly
XM_005267069.3:c.4868T>G	XP_005267126.2:p.Val1623Gly
XM_011535984.1:c.3947T>G	XP_011534286.1:p.Val1316Gly
XM_011535985.1:c.3767T>G	XP_011534287.1:p.Val1256Gly
XM_011535986.1:c.3527T>G	XP_011534288.1:p.Val1176Gly
XM_011535987.1:c.3146T>G	XP_011534289.1:p.Val1049Gly
XM_011535988.1:c.2009T>G	XP_011534290.1:p.Val670Gly
NM_001346813.1:c.4868T>G	NP_001333742.1:p.Val1623Gly
NM_001363725.1:c.2618T>G	NP_001350654.1:p.Val873Gly
XM_011535984.2:c.5078T>G	XP_011534286.2:p.Val1693Gly
XM_011535988.3:c.2009T>G	XP_011534290.1:p.Val670Gly
XM_017011103.2:c.4979T>G	XP_016866592.1:p.Val1660Gly
XM_017011104.1:c.4949T>G	XP_016866593.1:p.Val1650Gly
XM_017011105.2:c.4919T>G	XP_016866594.1:p.Val1640Gly
XM_017011106.2:c.4790T>G	XP_016866595.1:p.Val1597Gly
XM_017011107.2:c.4769T>G	XP_016866596.1:p.Val1590Gly
XR_002956289.1:n.5064T>G
NM_001363725.2:c.2618T>G	NP_001350654.1:p.Val873Gly
NM_001371656.1:c.4997T>G	NP_001358585.1:p.Val1666Gly
NM_001374820.1:c.4997T>G	NP_001361749.1:p.Val1666Gly
NM_001374828.1:c.5117T>G MANE Select	NP_001361757.1:p.Val1706Gly
NM_017519.3:c.4958T>G	NP_059989.3:p.Val1653Gly