Canonical Allele Identifier: CA366240887

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128372523
• MyVariant Identifiers: chr6:g.157521904C>A (hg19) ; chr6:g.157200770C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200770C>A , CM000668.2:g.157200770C>A	GRCh38
NC_000006.11:g.157521904C>A , CM000668.1:g.157521904C>A	GRCh37
NC_000006.10:g.157563596C>A	NCBI36
NG_032093.1:g.427841C>A
NG_032093.2:g.427841C>A
NG_066624.1:g.429745C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4386C>A	ENSP00000055163.8:p.Tyr1462Ter
ENST00000414678.8:c.4455C>A	ENSP00000412835.3:p.Tyr1485Ter
ENST00000637015.2:c.4674C>A	ENSP00000489729.2:p.Tyr1558Ter
ENST00000346085.10:c.4425C>A	ENSP00000344546.5:p.Tyr1475Ter
ENST00000350026.10:c.4137C>A	ENSP00000055163.7:p.Tyr1379Ter
ENST00000414678.7:c.2703C>A	ENSP00000412835.2:p.Tyr901Ter
ENST00000635849.1:c.1866C>A	ENSP00000490948.1:p.Tyr622Ter
ENST00000635957.1:c.1497C>A	ENSP00000490385.1:p.Tyr499Ter
ENST00000636227.1:n.3008C>A
ENST00000636254.1:n.465C>A
ENST00000636930.2:c.4545C>A MANE Select	ENSP00000490491.2:p.Tyr1515Ter
ENST00000636940.1:n.2542C>A
ENST00000637015.1:c.1913C>A
ENST00000637568.1:c.1827C>A
ENST00000637741.1:n.1211C>A
ENST00000637810.1:c.1887C>A	ENSP00000489636.1:p.Tyr629Ter
ENST00000637904.1:c.2046C>A	ENSP00000490550.1:p.Tyr682Ter
ENST00000647938.1:c.4176C>A	ENSP00000498155.1:p.Tyr1392Ter
ENST00000346085.9:c.4176C>A	ENSP00000344546.4:p.Tyr1392Ter
ENST00000350026.9:c.4137C>A	ENSP00000055163.7:p.Tyr1379Ter
ENST00000414678.6:c.2703C>A	ENSP00000412835.2:p.Tyr901Ter
NM_017519.2:c.4137C>A	NP_059989.2:p.Tyr1379Ter
NM_020732.3:c.4176C>A	NP_065783.3:p.Tyr1392Ter
XM_005267069.3:c.4296C>A	XP_005267126.2:p.Tyr1432Ter
XM_011535984.1:c.3375C>A	XP_011534286.1:p.Tyr1125Ter
XM_011535985.1:c.3195C>A	XP_011534287.1:p.Tyr1065Ter
XM_011535986.1:c.2955C>A	XP_011534288.1:p.Tyr985Ter
XM_011535987.1:c.2574C>A	XP_011534289.1:p.Tyr858Ter
XM_011535988.1:c.1437C>A	XP_011534290.1:p.Tyr479Ter
NM_001346813.1:c.4296C>A	NP_001333742.1:p.Tyr1432Ter
NM_001363725.1:c.2046C>A	NP_001350654.1:p.Tyr682Ter
XM_011535984.2:c.4506C>A	XP_011534286.2:p.Tyr1502Ter
XM_011535988.3:c.1437C>A	XP_011534290.1:p.Tyr479Ter
XM_017011103.2:c.4407C>A	XP_016866592.1:p.Tyr1469Ter
XM_017011104.1:c.4377C>A	XP_016866593.1:p.Tyr1459Ter
XM_017011105.2:c.4347C>A	XP_016866594.1:p.Tyr1449Ter
XM_017011106.2:c.4218C>A	XP_016866595.1:p.Tyr1406Ter
XM_017011107.2:c.4197C>A	XP_016866596.1:p.Tyr1399Ter
XR_002956289.1:n.4492C>A
NM_001363725.2:c.2046C>A	NP_001350654.1:p.Tyr682Ter
NM_001371656.1:c.4425C>A	NP_001358585.1:p.Tyr1475Ter
NM_001374820.1:c.4425C>A	NP_001361749.1:p.Tyr1475Ter
NM_001374828.1:c.4545C>A MANE Select	NP_001361757.1:p.Tyr1515Ter
NM_017519.3:c.4386C>A	NP_059989.3:p.Tyr1462Ter