Canonical Allele Identifier: CA366239586

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519967T>G (hg19) ; chr6:g.157198833T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198833T>G , CM000668.2:g.157198833T>G	GRCh38
NC_000006.11:g.157519967T>G , CM000668.1:g.157519967T>G	GRCh37
NC_000006.10:g.157561659T>G	NCBI36
NG_032093.1:g.425904T>G
NG_032093.2:g.425904T>G
NG_066624.1:g.427808T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4246T>G	ENSP00000055163.8:p.Tyr1416Asp
ENST00000414678.8:c.4315T>G	ENSP00000412835.3:p.Tyr1439Asp
ENST00000637015.2:c.4534T>G	ENSP00000489729.2:p.Tyr1512Asp
ENST00000346085.10:c.4285T>G	ENSP00000344546.5:p.Tyr1429Asp
ENST00000350026.10:c.3997T>G	ENSP00000055163.7:p.Tyr1333Asp
ENST00000414678.7:c.2563T>G	ENSP00000412835.2:p.Tyr855Asp
ENST00000635849.1:c.1726T>G	ENSP00000490948.1:p.Tyr576Asp
ENST00000635957.1:c.1357T>G	ENSP00000490385.1:p.Tyr453Asp
ENST00000636227.1:n.2868T>G
ENST00000636254.1:n.325T>G
ENST00000636930.2:c.4405T>G MANE Select	ENSP00000490491.2:p.Tyr1469Asp
ENST00000636940.1:n.2402T>G
ENST00000637015.1:c.1773T>G
ENST00000637568.1:c.1687T>G
ENST00000637741.1:n.1071T>G
ENST00000637810.1:c.1747T>G	ENSP00000489636.1:p.Tyr583Asp
ENST00000637904.1:c.1906T>G	ENSP00000490550.1:p.Tyr636Asp
ENST00000647938.1:c.4036T>G	ENSP00000498155.1:p.Tyr1346Asp
ENST00000346085.9:c.4036T>G	ENSP00000344546.4:p.Tyr1346Asp
ENST00000350026.9:c.3997T>G	ENSP00000055163.7:p.Tyr1333Asp
ENST00000414678.6:c.2563T>G	ENSP00000412835.2:p.Tyr855Asp
NM_017519.2:c.3997T>G	NP_059989.2:p.Tyr1333Asp
NM_020732.3:c.4036T>G	NP_065783.3:p.Tyr1346Asp
XM_005267069.3:c.4156T>G	XP_005267126.2:p.Tyr1386Asp
XM_011535984.1:c.3235T>G	XP_011534286.1:p.Tyr1079Asp
XM_011535985.1:c.3055T>G	XP_011534287.1:p.Tyr1019Asp
XM_011535986.1:c.2815T>G	XP_011534288.1:p.Tyr939Asp
XM_011535987.1:c.2434T>G	XP_011534289.1:p.Tyr812Asp
XM_011535988.1:c.1297T>G	XP_011534290.1:p.Tyr433Asp
NM_001346813.1:c.4156T>G	NP_001333742.1:p.Tyr1386Asp
NM_001363725.1:c.1906T>G	NP_001350654.1:p.Tyr636Asp
XM_011535984.2:c.4366T>G	XP_011534286.2:p.Tyr1456Asp
XM_011535988.3:c.1297T>G	XP_011534290.1:p.Tyr433Asp
XM_017011103.2:c.4267T>G	XP_016866592.1:p.Tyr1423Asp
XM_017011104.1:c.4237T>G	XP_016866593.1:p.Tyr1413Asp
XM_017011105.2:c.4207T>G	XP_016866594.1:p.Tyr1403Asp
XM_017011106.2:c.4078T>G	XP_016866595.1:p.Tyr1360Asp
XM_017011107.2:c.4057T>G	XP_016866596.1:p.Tyr1353Asp
XR_002956289.1:n.4427-1872T>G
NM_001363725.2:c.1906T>G	NP_001350654.1:p.Tyr636Asp
NM_001371656.1:c.4285T>G	NP_001358585.1:p.Tyr1429Asp
NM_001374820.1:c.4285T>G	NP_001361749.1:p.Tyr1429Asp
NM_001374828.1:c.4405T>G MANE Select	NP_001361757.1:p.Tyr1469Asp
NM_017519.3:c.4246T>G	NP_059989.3:p.Tyr1416Asp