Canonical Allele Identifier: CA366242094

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522275T>G (hg19) ; chr6:g.157201141T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201141T>G , CM000668.2:g.157201141T>G	GRCh38
NC_000006.11:g.157522275T>G , CM000668.1:g.157522275T>G	GRCh37
NC_000006.10:g.157563967T>G	NCBI36
NG_032093.1:g.428212T>G
NG_032093.2:g.428212T>G
NG_066624.1:g.430116T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4757T>G	ENSP00000055163.8:p.Val1586Gly
ENST00000414678.8:c.4826T>G	ENSP00000412835.3:p.Val1609Gly
ENST00000637015.2:c.5045T>G	ENSP00000489729.2:p.Val1682Gly
ENST00000346085.10:c.4796T>G	ENSP00000344546.5:p.Val1599Gly
ENST00000350026.10:c.4508T>G	ENSP00000055163.7:p.Val1503Gly
ENST00000414678.7:c.3074T>G	ENSP00000412835.2:p.Val1025Gly
ENST00000635849.1:c.2237T>G	ENSP00000490948.1:p.Val746Gly
ENST00000635957.1:c.1868T>G	ENSP00000490385.1:p.Val623Gly
ENST00000636227.1:n.3379T>G
ENST00000636254.1:n.836T>G
ENST00000636930.2:c.4916T>G MANE Select	ENSP00000490491.2:p.Val1639Gly
ENST00000636940.1:n.2913T>G
ENST00000637015.1:c.2284T>G
ENST00000637568.1:c.2198T>G
ENST00000637741.1:n.1582T>G
ENST00000637810.1:c.2258T>G	ENSP00000489636.1:p.Val753Gly
ENST00000637904.1:c.2417T>G	ENSP00000490550.1:p.Val806Gly
ENST00000647938.1:c.4547T>G	ENSP00000498155.1:p.Val1516Gly
ENST00000346085.9:c.4547T>G	ENSP00000344546.4:p.Val1516Gly
ENST00000350026.9:c.4508T>G	ENSP00000055163.7:p.Val1503Gly
ENST00000414678.6:c.3074T>G	ENSP00000412835.2:p.Val1025Gly
NM_017519.2:c.4508T>G	NP_059989.2:p.Val1503Gly
NM_020732.3:c.4547T>G	NP_065783.3:p.Val1516Gly
XM_005267069.3:c.4667T>G	XP_005267126.2:p.Val1556Gly
XM_011535984.1:c.3746T>G	XP_011534286.1:p.Val1249Gly
XM_011535985.1:c.3566T>G	XP_011534287.1:p.Val1189Gly
XM_011535986.1:c.3326T>G	XP_011534288.1:p.Val1109Gly
XM_011535987.1:c.2945T>G	XP_011534289.1:p.Val982Gly
XM_011535988.1:c.1808T>G	XP_011534290.1:p.Val603Gly
NM_001346813.1:c.4667T>G	NP_001333742.1:p.Val1556Gly
NM_001363725.1:c.2417T>G	NP_001350654.1:p.Val806Gly
XM_011535984.2:c.4877T>G	XP_011534286.2:p.Val1626Gly
XM_011535988.3:c.1808T>G	XP_011534290.1:p.Val603Gly
XM_017011103.2:c.4778T>G	XP_016866592.1:p.Val1593Gly
XM_017011104.1:c.4748T>G	XP_016866593.1:p.Val1583Gly
XM_017011105.2:c.4718T>G	XP_016866594.1:p.Val1573Gly
XM_017011106.2:c.4589T>G	XP_016866595.1:p.Val1530Gly
XM_017011107.2:c.4568T>G	XP_016866596.1:p.Val1523Gly
XR_002956289.1:n.4863T>G
NM_001363725.2:c.2417T>G	NP_001350654.1:p.Val806Gly
NM_001371656.1:c.4796T>G	NP_001358585.1:p.Val1599Gly
NM_001374820.1:c.4796T>G	NP_001361749.1:p.Val1599Gly
NM_001374828.1:c.4916T>G MANE Select	NP_001361757.1:p.Val1639Gly
NM_017519.3:c.4757T>G	NP_059989.3:p.Val1586Gly