Canonical Allele Identifier: CA366239817

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366511
• MyVariant Identifiers: chr6:g.157520016A>T (hg19) ; chr6:g.157198882A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198882A>T , CM000668.2:g.157198882A>T	GRCh38
NC_000006.11:g.157520016A>T , CM000668.1:g.157520016A>T	GRCh37
NC_000006.10:g.157561708A>T	NCBI36
NG_032093.1:g.425953A>T
NG_032093.2:g.425953A>T
NG_066624.1:g.427857A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4295A>T	ENSP00000055163.8:p.Gln1432Leu
ENST00000414678.8:c.4364A>T	ENSP00000412835.3:p.Gln1455Leu
ENST00000637015.2:c.4583A>T	ENSP00000489729.2:p.Gln1528Leu
ENST00000346085.10:c.4334A>T	ENSP00000344546.5:p.Gln1445Leu
ENST00000350026.10:c.4046A>T	ENSP00000055163.7:p.Gln1349Leu
ENST00000414678.7:c.2612A>T	ENSP00000412835.2:p.Gln871Leu
ENST00000635849.1:c.1775A>T	ENSP00000490948.1:p.Gln592Leu
ENST00000635957.1:c.1406A>T	ENSP00000490385.1:p.Gln469Leu
ENST00000636227.1:n.2917A>T
ENST00000636254.1:n.374A>T
ENST00000636930.2:c.4454A>T MANE Select	ENSP00000490491.2:p.Gln1485Leu
ENST00000636940.1:n.2451A>T
ENST00000637015.1:c.1822A>T
ENST00000637568.1:c.1736A>T
ENST00000637741.1:n.1120A>T
ENST00000637810.1:c.1796A>T	ENSP00000489636.1:p.Gln599Leu
ENST00000637904.1:c.1955A>T	ENSP00000490550.1:p.Gln652Leu
ENST00000647938.1:c.4085A>T	ENSP00000498155.1:p.Gln1362Leu
ENST00000346085.9:c.4085A>T	ENSP00000344546.4:p.Gln1362Leu
ENST00000350026.9:c.4046A>T	ENSP00000055163.7:p.Gln1349Leu
ENST00000414678.6:c.2612A>T	ENSP00000412835.2:p.Gln871Leu
NM_017519.2:c.4046A>T	NP_059989.2:p.Gln1349Leu
NM_020732.3:c.4085A>T	NP_065783.3:p.Gln1362Leu
XM_005267069.3:c.4205A>T	XP_005267126.2:p.Gln1402Leu
XM_011535984.1:c.3284A>T	XP_011534286.1:p.Gln1095Leu
XM_011535985.1:c.3104A>T	XP_011534287.1:p.Gln1035Leu
XM_011535986.1:c.2864A>T	XP_011534288.1:p.Gln955Leu
XM_011535987.1:c.2483A>T	XP_011534289.1:p.Gln828Leu
XM_011535988.1:c.1346A>T	XP_011534290.1:p.Gln449Leu
NM_001346813.1:c.4205A>T	NP_001333742.1:p.Gln1402Leu
NM_001363725.1:c.1955A>T	NP_001350654.1:p.Gln652Leu
XM_011535984.2:c.4415A>T	XP_011534286.2:p.Gln1472Leu
XM_011535988.3:c.1346A>T	XP_011534290.1:p.Gln449Leu
XM_017011103.2:c.4316A>T	XP_016866592.1:p.Gln1439Leu
XM_017011104.1:c.4286A>T	XP_016866593.1:p.Gln1429Leu
XM_017011105.2:c.4256A>T	XP_016866594.1:p.Gln1419Leu
XM_017011106.2:c.4127A>T	XP_016866595.1:p.Gln1376Leu
XM_017011107.2:c.4106A>T	XP_016866596.1:p.Gln1369Leu
XR_002956289.1:n.4427-1823A>T
NM_001363725.2:c.1955A>T	NP_001350654.1:p.Gln652Leu
NM_001371656.1:c.4334A>T	NP_001358585.1:p.Gln1445Leu
NM_001374820.1:c.4334A>T	NP_001361749.1:p.Gln1445Leu
NM_001374828.1:c.4454A>T MANE Select	NP_001361757.1:p.Gln1485Leu
NM_017519.3:c.4295A>T	NP_059989.3:p.Gln1432Leu