Canonical Allele Identifier: CA366240882

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128372515
• MyVariant Identifiers: chr6:g.157521902T>G (hg19) ; chr6:g.157200768T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200768T>G , CM000668.2:g.157200768T>G	GRCh38
NC_000006.11:g.157521902T>G , CM000668.1:g.157521902T>G	GRCh37
NC_000006.10:g.157563594T>G	NCBI36
NG_032093.1:g.427839T>G
NG_032093.2:g.427839T>G
NG_066624.1:g.429743T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4384T>G	ENSP00000055163.8:p.Tyr1462Asp
ENST00000414678.8:c.4453T>G	ENSP00000412835.3:p.Tyr1485Asp
ENST00000637015.2:c.4672T>G	ENSP00000489729.2:p.Tyr1558Asp
ENST00000346085.10:c.4423T>G	ENSP00000344546.5:p.Tyr1475Asp
ENST00000350026.10:c.4135T>G	ENSP00000055163.7:p.Tyr1379Asp
ENST00000414678.7:c.2701T>G	ENSP00000412835.2:p.Tyr901Asp
ENST00000635849.1:c.1864T>G	ENSP00000490948.1:p.Tyr622Asp
ENST00000635957.1:c.1495T>G	ENSP00000490385.1:p.Tyr499Asp
ENST00000636227.1:n.3006T>G
ENST00000636254.1:n.463T>G
ENST00000636930.2:c.4543T>G MANE Select	ENSP00000490491.2:p.Tyr1515Asp
ENST00000636940.1:n.2540T>G
ENST00000637015.1:c.1911T>G
ENST00000637568.1:c.1825T>G
ENST00000637741.1:n.1209T>G
ENST00000637810.1:c.1885T>G	ENSP00000489636.1:p.Tyr629Asp
ENST00000637904.1:c.2044T>G	ENSP00000490550.1:p.Tyr682Asp
ENST00000647938.1:c.4174T>G	ENSP00000498155.1:p.Tyr1392Asp
ENST00000346085.9:c.4174T>G	ENSP00000344546.4:p.Tyr1392Asp
ENST00000350026.9:c.4135T>G	ENSP00000055163.7:p.Tyr1379Asp
ENST00000414678.6:c.2701T>G	ENSP00000412835.2:p.Tyr901Asp
NM_017519.2:c.4135T>G	NP_059989.2:p.Tyr1379Asp
NM_020732.3:c.4174T>G	NP_065783.3:p.Tyr1392Asp
XM_005267069.3:c.4294T>G	XP_005267126.2:p.Tyr1432Asp
XM_011535984.1:c.3373T>G	XP_011534286.1:p.Tyr1125Asp
XM_011535985.1:c.3193T>G	XP_011534287.1:p.Tyr1065Asp
XM_011535986.1:c.2953T>G	XP_011534288.1:p.Tyr985Asp
XM_011535987.1:c.2572T>G	XP_011534289.1:p.Tyr858Asp
XM_011535988.1:c.1435T>G	XP_011534290.1:p.Tyr479Asp
NM_001346813.1:c.4294T>G	NP_001333742.1:p.Tyr1432Asp
NM_001363725.1:c.2044T>G	NP_001350654.1:p.Tyr682Asp
XM_011535984.2:c.4504T>G	XP_011534286.2:p.Tyr1502Asp
XM_011535988.3:c.1435T>G	XP_011534290.1:p.Tyr479Asp
XM_017011103.2:c.4405T>G	XP_016866592.1:p.Tyr1469Asp
XM_017011104.1:c.4375T>G	XP_016866593.1:p.Tyr1459Asp
XM_017011105.2:c.4345T>G	XP_016866594.1:p.Tyr1449Asp
XM_017011106.2:c.4216T>G	XP_016866595.1:p.Tyr1406Asp
XM_017011107.2:c.4195T>G	XP_016866596.1:p.Tyr1399Asp
XR_002956289.1:n.4490T>G
NM_001363725.2:c.2044T>G	NP_001350654.1:p.Tyr682Asp
NM_001371656.1:c.4423T>G	NP_001358585.1:p.Tyr1475Asp
NM_001374820.1:c.4423T>G	NP_001361749.1:p.Tyr1475Asp
NM_001374828.1:c.4543T>G MANE Select	NP_001361757.1:p.Tyr1515Asp
NM_017519.3:c.4384T>G	NP_059989.3:p.Tyr1462Asp