Canonical Allele Identifier: CA366241391

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128373852
• MyVariant Identifiers: chr6:g.157522127G>A (hg19) ; chr6:g.157200993G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200993G>A , CM000668.2:g.157200993G>A	GRCh38
NC_000006.11:g.157522127G>A , CM000668.1:g.157522127G>A	GRCh37
NC_000006.10:g.157563819G>A	NCBI36
NG_032093.1:g.428064G>A
NG_032093.2:g.428064G>A
NG_066624.1:g.429968G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4609G>A	ENSP00000055163.8:p.Ala1537Thr
ENST00000414678.8:c.4678G>A	ENSP00000412835.3:p.Ala1560Thr
ENST00000637015.2:c.4897G>A	ENSP00000489729.2:p.Ala1633Thr
ENST00000346085.10:c.4648G>A	ENSP00000344546.5:p.Ala1550Thr
ENST00000350026.10:c.4360G>A	ENSP00000055163.7:p.Ala1454Thr
ENST00000414678.7:c.2926G>A	ENSP00000412835.2:p.Ala976Thr
ENST00000635849.1:c.2089G>A	ENSP00000490948.1:p.Ala697Thr
ENST00000635957.1:c.1720G>A	ENSP00000490385.1:p.Ala574Thr
ENST00000636227.1:n.3231G>A
ENST00000636254.1:n.688G>A
ENST00000636930.2:c.4768G>A MANE Select	ENSP00000490491.2:p.Ala1590Thr
ENST00000636940.1:n.2765G>A
ENST00000637015.1:c.2136G>A
ENST00000637568.1:c.2050G>A
ENST00000637741.1:n.1434G>A
ENST00000637810.1:c.2110G>A	ENSP00000489636.1:p.Ala704Thr
ENST00000637904.1:c.2269G>A	ENSP00000490550.1:p.Ala757Thr
ENST00000647938.1:c.4399G>A	ENSP00000498155.1:p.Ala1467Thr
ENST00000346085.9:c.4399G>A	ENSP00000344546.4:p.Ala1467Thr
ENST00000350026.9:c.4360G>A	ENSP00000055163.7:p.Ala1454Thr
ENST00000414678.6:c.2926G>A	ENSP00000412835.2:p.Ala976Thr
NM_017519.2:c.4360G>A	NP_059989.2:p.Ala1454Thr
NM_020732.3:c.4399G>A	NP_065783.3:p.Ala1467Thr
XM_005267069.3:c.4519G>A	XP_005267126.2:p.Ala1507Thr
XM_011535984.1:c.3598G>A	XP_011534286.1:p.Ala1200Thr
XM_011535985.1:c.3418G>A	XP_011534287.1:p.Ala1140Thr
XM_011535986.1:c.3178G>A	XP_011534288.1:p.Ala1060Thr
XM_011535987.1:c.2797G>A	XP_011534289.1:p.Ala933Thr
XM_011535988.1:c.1660G>A	XP_011534290.1:p.Ala554Thr
NM_001346813.1:c.4519G>A	NP_001333742.1:p.Ala1507Thr
NM_001363725.1:c.2269G>A	NP_001350654.1:p.Ala757Thr
XM_011535984.2:c.4729G>A	XP_011534286.2:p.Ala1577Thr
XM_011535988.3:c.1660G>A	XP_011534290.1:p.Ala554Thr
XM_017011103.2:c.4630G>A	XP_016866592.1:p.Ala1544Thr
XM_017011104.1:c.4600G>A	XP_016866593.1:p.Ala1534Thr
XM_017011105.2:c.4570G>A	XP_016866594.1:p.Ala1524Thr
XM_017011106.2:c.4441G>A	XP_016866595.1:p.Ala1481Thr
XM_017011107.2:c.4420G>A	XP_016866596.1:p.Ala1474Thr
XR_002956289.1:n.4715G>A
NM_001363725.2:c.2269G>A	NP_001350654.1:p.Ala757Thr
NM_001371656.1:c.4648G>A	NP_001358585.1:p.Ala1550Thr
NM_001374820.1:c.4648G>A	NP_001361749.1:p.Ala1550Thr
NM_001374828.1:c.4768G>A MANE Select	NP_001361757.1:p.Ala1590Thr
NM_017519.3:c.4609G>A	NP_059989.3:p.Ala1537Thr