Canonical Allele Identifier: CA366235301

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511249C>A (hg19) ; chr6:g.157190115C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190115C>A , CM000668.2:g.157190115C>A	GRCh38
NC_000006.11:g.157511249C>A , CM000668.1:g.157511249C>A	GRCh37
NC_000006.10:g.157552941C>A	NCBI36
NG_032093.1:g.417186C>A
NG_032093.2:g.417186C>A
NG_066624.1:g.419090C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3977C>A	ENSP00000055163.8:p.Pro1326Gln
ENST00000414678.8:c.4046C>A	ENSP00000412835.3:p.Pro1349Gln
ENST00000637015.2:c.4265C>A	ENSP00000489729.2:p.Pro1422Gln
ENST00000346085.10:c.4016C>A	ENSP00000344546.5:p.Pro1339Gln
ENST00000350026.10:c.3728C>A	ENSP00000055163.7:p.Pro1243Gln
ENST00000414678.7:c.2294C>A	ENSP00000412835.2:p.Pro765Gln
ENST00000635849.1:c.1457C>A	ENSP00000490948.1:p.Pro486Gln
ENST00000635957.1:c.1088C>A	ENSP00000490385.1:p.Pro363Gln
ENST00000636930.2:c.4136C>A MANE Select	ENSP00000490491.2:p.Pro1379Gln
ENST00000636940.1:n.2133C>A
ENST00000637015.1:c.1504C>A
ENST00000637568.1:c.1418C>A
ENST00000637741.1:n.802C>A
ENST00000637810.1:c.1478C>A	ENSP00000489636.1:p.Pro493Gln
ENST00000637904.1:c.1637C>A	ENSP00000490550.1:p.Pro546Gln
ENST00000647938.1:c.3767C>A	ENSP00000498155.1:p.Pro1256Gln
ENST00000346085.9:c.3767C>A	ENSP00000344546.4:p.Pro1256Gln
ENST00000350026.9:c.3728C>A	ENSP00000055163.7:p.Pro1243Gln
ENST00000414678.6:c.2294C>A	ENSP00000412835.2:p.Pro765Gln
NM_017519.2:c.3728C>A	NP_059989.2:p.Pro1243Gln
NM_020732.3:c.3767C>A	NP_065783.3:p.Pro1256Gln
XM_005267069.3:c.3887C>A	XP_005267126.2:p.Pro1296Gln
XM_011535984.1:c.2966C>A	XP_011534286.1:p.Pro989Gln
XM_011535985.1:c.2786C>A	XP_011534287.1:p.Pro929Gln
XM_011535986.1:c.2546C>A	XP_011534288.1:p.Pro849Gln
XM_011535987.1:c.2165C>A	XP_011534289.1:p.Pro722Gln
XM_011535988.1:c.1028C>A	XP_011534290.1:p.Pro343Gln
NM_001346813.1:c.3887C>A	NP_001333742.1:p.Pro1296Gln
NM_001363725.1:c.1637C>A	NP_001350654.1:p.Pro546Gln
XM_011535984.2:c.4097C>A	XP_011534286.2:p.Pro1366Gln
XM_011535988.3:c.1028C>A	XP_011534290.1:p.Pro343Gln
XM_017011103.2:c.3998C>A	XP_016866592.1:p.Pro1333Gln
XM_017011104.1:c.3968C>A	XP_016866593.1:p.Pro1323Gln
XM_017011105.2:c.3938C>A	XP_016866594.1:p.Pro1313Gln
XM_017011106.2:c.3809C>A	XP_016866595.1:p.Pro1270Gln
XM_017011107.2:c.3788C>A	XP_016866596.1:p.Pro1263Gln
XR_002956289.1:n.4180C>A
NM_001363725.2:c.1637C>A	NP_001350654.1:p.Pro546Gln
NM_001371656.1:c.4016C>A	NP_001358585.1:p.Pro1339Gln
NM_001374820.1:c.4016C>A	NP_001361749.1:p.Pro1339Gln
NM_001374828.1:c.4136C>A MANE Select	NP_001361757.1:p.Pro1379Gln
NM_017519.3:c.3977C>A	NP_059989.3:p.Pro1326Gln