Canonical Allele Identifier: CA366241488

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522145T>G (hg19) ; chr6:g.157201011T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201011T>G , CM000668.2:g.157201011T>G	GRCh38
NC_000006.11:g.157522145T>G , CM000668.1:g.157522145T>G	GRCh37
NC_000006.10:g.157563837T>G	NCBI36
NG_032093.1:g.428082T>G
NG_032093.2:g.428082T>G
NG_066624.1:g.429986T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4627T>G	ENSP00000055163.8:p.Tyr1543Asp
ENST00000414678.8:c.4696T>G	ENSP00000412835.3:p.Tyr1566Asp
ENST00000637015.2:c.4915T>G	ENSP00000489729.2:p.Tyr1639Asp
ENST00000346085.10:c.4666T>G	ENSP00000344546.5:p.Tyr1556Asp
ENST00000350026.10:c.4378T>G	ENSP00000055163.7:p.Tyr1460Asp
ENST00000414678.7:c.2944T>G	ENSP00000412835.2:p.Tyr982Asp
ENST00000635849.1:c.2107T>G	ENSP00000490948.1:p.Tyr703Asp
ENST00000635957.1:c.1738T>G	ENSP00000490385.1:p.Tyr580Asp
ENST00000636227.1:n.3249T>G
ENST00000636254.1:n.706T>G
ENST00000636930.2:c.4786T>G MANE Select	ENSP00000490491.2:p.Tyr1596Asp
ENST00000636940.1:n.2783T>G
ENST00000637015.1:c.2154T>G
ENST00000637568.1:c.2068T>G
ENST00000637741.1:n.1452T>G
ENST00000637810.1:c.2128T>G	ENSP00000489636.1:p.Tyr710Asp
ENST00000637904.1:c.2287T>G	ENSP00000490550.1:p.Tyr763Asp
ENST00000647938.1:c.4417T>G	ENSP00000498155.1:p.Tyr1473Asp
ENST00000346085.9:c.4417T>G	ENSP00000344546.4:p.Tyr1473Asp
ENST00000350026.9:c.4378T>G	ENSP00000055163.7:p.Tyr1460Asp
ENST00000414678.6:c.2944T>G	ENSP00000412835.2:p.Tyr982Asp
NM_017519.2:c.4378T>G	NP_059989.2:p.Tyr1460Asp
NM_020732.3:c.4417T>G	NP_065783.3:p.Tyr1473Asp
XM_005267069.3:c.4537T>G	XP_005267126.2:p.Tyr1513Asp
XM_011535984.1:c.3616T>G	XP_011534286.1:p.Tyr1206Asp
XM_011535985.1:c.3436T>G	XP_011534287.1:p.Tyr1146Asp
XM_011535986.1:c.3196T>G	XP_011534288.1:p.Tyr1066Asp
XM_011535987.1:c.2815T>G	XP_011534289.1:p.Tyr939Asp
XM_011535988.1:c.1678T>G	XP_011534290.1:p.Tyr560Asp
NM_001346813.1:c.4537T>G	NP_001333742.1:p.Tyr1513Asp
NM_001363725.1:c.2287T>G	NP_001350654.1:p.Tyr763Asp
XM_011535984.2:c.4747T>G	XP_011534286.2:p.Tyr1583Asp
XM_011535988.3:c.1678T>G	XP_011534290.1:p.Tyr560Asp
XM_017011103.2:c.4648T>G	XP_016866592.1:p.Tyr1550Asp
XM_017011104.1:c.4618T>G	XP_016866593.1:p.Tyr1540Asp
XM_017011105.2:c.4588T>G	XP_016866594.1:p.Tyr1530Asp
XM_017011106.2:c.4459T>G	XP_016866595.1:p.Tyr1487Asp
XM_017011107.2:c.4438T>G	XP_016866596.1:p.Tyr1480Asp
XR_002956289.1:n.4733T>G
NM_001363725.2:c.2287T>G	NP_001350654.1:p.Tyr763Asp
NM_001371656.1:c.4666T>G	NP_001358585.1:p.Tyr1556Asp
NM_001374820.1:c.4666T>G	NP_001361749.1:p.Tyr1556Asp
NM_001374828.1:c.4786T>G MANE Select	NP_001361757.1:p.Tyr1596Asp
NM_017519.3:c.4627T>G	NP_059989.3:p.Tyr1543Asp