Canonical Allele Identifier: CA366241882

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794073907
• MyVariant Identifiers: chr6:g.157522217G>A (hg19) ; chr6:g.157201083G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201083G>A , CM000668.2:g.157201083G>A	GRCh38
NC_000006.11:g.157522217G>A , CM000668.1:g.157522217G>A	GRCh37
NC_000006.10:g.157563909G>A	NCBI36
NG_032093.1:g.428154G>A
NG_032093.2:g.428154G>A
NG_066624.1:g.430058G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4699G>A	ENSP00000055163.8:p.Asp1567Asn
ENST00000414678.8:c.4768G>A	ENSP00000412835.3:p.Asp1590Asn
ENST00000637015.2:c.4987G>A	ENSP00000489729.2:p.Asp1663Asn
ENST00000346085.10:c.4738G>A	ENSP00000344546.5:p.Asp1580Asn
ENST00000350026.10:c.4450G>A	ENSP00000055163.7:p.Asp1484Asn
ENST00000414678.7:c.3016G>A	ENSP00000412835.2:p.Asp1006Asn
ENST00000635849.1:c.2179G>A	ENSP00000490948.1:p.Asp727Asn
ENST00000635957.1:c.1810G>A	ENSP00000490385.1:p.Asp604Asn
ENST00000636227.1:n.3321G>A
ENST00000636254.1:n.778G>A
ENST00000636930.2:c.4858G>A MANE Select	ENSP00000490491.2:p.Asp1620Asn
ENST00000636940.1:n.2855G>A
ENST00000637015.1:c.2226G>A
ENST00000637568.1:c.2140G>A
ENST00000637741.1:n.1524G>A
ENST00000637810.1:c.2200G>A	ENSP00000489636.1:p.Asp734Asn
ENST00000637904.1:c.2359G>A	ENSP00000490550.1:p.Asp787Asn
ENST00000647938.1:c.4489G>A	ENSP00000498155.1:p.Asp1497Asn
ENST00000346085.9:c.4489G>A	ENSP00000344546.4:p.Asp1497Asn
ENST00000350026.9:c.4450G>A	ENSP00000055163.7:p.Asp1484Asn
ENST00000414678.6:c.3016G>A	ENSP00000412835.2:p.Asp1006Asn
NM_017519.2:c.4450G>A	NP_059989.2:p.Asp1484Asn
NM_020732.3:c.4489G>A	NP_065783.3:p.Asp1497Asn
XM_005267069.3:c.4609G>A	XP_005267126.2:p.Asp1537Asn
XM_011535984.1:c.3688G>A	XP_011534286.1:p.Asp1230Asn
XM_011535985.1:c.3508G>A	XP_011534287.1:p.Asp1170Asn
XM_011535986.1:c.3268G>A	XP_011534288.1:p.Asp1090Asn
XM_011535987.1:c.2887G>A	XP_011534289.1:p.Asp963Asn
XM_011535988.1:c.1750G>A	XP_011534290.1:p.Asp584Asn
NM_001346813.1:c.4609G>A	NP_001333742.1:p.Asp1537Asn
NM_001363725.1:c.2359G>A	NP_001350654.1:p.Asp787Asn
XM_011535984.2:c.4819G>A	XP_011534286.2:p.Asp1607Asn
XM_011535988.3:c.1750G>A	XP_011534290.1:p.Asp584Asn
XM_017011103.2:c.4720G>A	XP_016866592.1:p.Asp1574Asn
XM_017011104.1:c.4690G>A	XP_016866593.1:p.Asp1564Asn
XM_017011105.2:c.4660G>A	XP_016866594.1:p.Asp1554Asn
XM_017011106.2:c.4531G>A	XP_016866595.1:p.Asp1511Asn
XM_017011107.2:c.4510G>A	XP_016866596.1:p.Asp1504Asn
XR_002956289.1:n.4805G>A
NM_001363725.2:c.2359G>A	NP_001350654.1:p.Asp787Asn
NM_001371656.1:c.4738G>A	NP_001358585.1:p.Asp1580Asn
NM_001374820.1:c.4738G>A	NP_001361749.1:p.Asp1580Asn
NM_001374828.1:c.4858G>A MANE Select	NP_001361757.1:p.Asp1620Asn
NM_017519.3:c.4699G>A	NP_059989.3:p.Asp1567Asn