Canonical Allele Identifier: CA366240881

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4384T>A	ENSP00000055163.8:p.Tyr1462Asn
ENST00000414678.8:c.4453T>A	ENSP00000412835.3:p.Tyr1485Asn
ENST00000637015.2:c.4672T>A	ENSP00000489729.2:p.Tyr1558Asn
ENST00000346085.10:c.4423T>A	ENSP00000344546.5:p.Tyr1475Asn
ENST00000350026.10:c.4135T>A	ENSP00000055163.7:p.Tyr1379Asn
ENST00000414678.7:c.2701T>A	ENSP00000412835.2:p.Tyr901Asn
ENST00000635849.1:c.1864T>A	ENSP00000490948.1:p.Tyr622Asn
ENST00000635957.1:c.1495T>A	ENSP00000490385.1:p.Tyr499Asn
ENST00000636227.1:n.3006T>A
ENST00000636254.1:n.463T>A
ENST00000636930.2:c.4543T>A MANE Select	ENSP00000490491.2:p.Tyr1515Asn
ENST00000636940.1:n.2540T>A
ENST00000637015.1:c.1911T>A
ENST00000637568.1:c.1825T>A
ENST00000637741.1:n.1209T>A
ENST00000637810.1:c.1885T>A	ENSP00000489636.1:p.Tyr629Asn
ENST00000637904.1:c.2044T>A	ENSP00000490550.1:p.Tyr682Asn
ENST00000647938.1:c.4174T>A	ENSP00000498155.1:p.Tyr1392Asn
ENST00000346085.9:c.4174T>A	ENSP00000344546.4:p.Tyr1392Asn
ENST00000350026.9:c.4135T>A	ENSP00000055163.7:p.Tyr1379Asn
ENST00000414678.6:c.2701T>A	ENSP00000412835.2:p.Tyr901Asn
NM_017519.2:c.4135T>A	NP_059989.2:p.Tyr1379Asn
NM_020732.3:c.4174T>A	NP_065783.3:p.Tyr1392Asn
XM_005267069.3:c.4294T>A	XP_005267126.2:p.Tyr1432Asn
XM_011535984.1:c.3373T>A	XP_011534286.1:p.Tyr1125Asn
XM_011535985.1:c.3193T>A	XP_011534287.1:p.Tyr1065Asn
XM_011535986.1:c.2953T>A	XP_011534288.1:p.Tyr985Asn
XM_011535987.1:c.2572T>A	XP_011534289.1:p.Tyr858Asn
XM_011535988.1:c.1435T>A	XP_011534290.1:p.Tyr479Asn
NM_001346813.1:c.4294T>A	NP_001333742.1:p.Tyr1432Asn
NM_001363725.1:c.2044T>A	NP_001350654.1:p.Tyr682Asn
XM_011535984.2:c.4504T>A	XP_011534286.2:p.Tyr1502Asn
XM_011535988.3:c.1435T>A	XP_011534290.1:p.Tyr479Asn
XM_017011103.2:c.4405T>A	XP_016866592.1:p.Tyr1469Asn
XM_017011104.1:c.4375T>A	XP_016866593.1:p.Tyr1459Asn
XM_017011105.2:c.4345T>A	XP_016866594.1:p.Tyr1449Asn
XM_017011106.2:c.4216T>A	XP_016866595.1:p.Tyr1406Asn
XM_017011107.2:c.4195T>A	XP_016866596.1:p.Tyr1399Asn
XR_002956289.1:n.4490T>A
NM_001363725.2:c.2044T>A	NP_001350654.1:p.Tyr682Asn
NM_001371656.1:c.4423T>A	NP_001358585.1:p.Tyr1475Asn
NM_001374820.1:c.4423T>A	NP_001361749.1:p.Tyr1475Asn
NM_001374828.1:c.4543T>A MANE Select	NP_001361757.1:p.Tyr1515Asn
NM_017519.3:c.4384T>A	NP_059989.3:p.Tyr1462Asn