Canonical Allele Identifier: CA366235302

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3977C>G	ENSP00000055163.8:p.Pro1326Arg
ENST00000414678.8:c.4046C>G	ENSP00000412835.3:p.Pro1349Arg
ENST00000637015.2:c.4265C>G	ENSP00000489729.2:p.Pro1422Arg
ENST00000346085.10:c.4016C>G	ENSP00000344546.5:p.Pro1339Arg
ENST00000350026.10:c.3728C>G	ENSP00000055163.7:p.Pro1243Arg
ENST00000414678.7:c.2294C>G	ENSP00000412835.2:p.Pro765Arg
ENST00000635849.1:c.1457C>G	ENSP00000490948.1:p.Pro486Arg
ENST00000635957.1:c.1088C>G	ENSP00000490385.1:p.Pro363Arg
ENST00000636930.2:c.4136C>G MANE Select	ENSP00000490491.2:p.Pro1379Arg
ENST00000636940.1:n.2133C>G
ENST00000637015.1:c.1504C>G
ENST00000637568.1:c.1418C>G
ENST00000637741.1:n.802C>G
ENST00000637810.1:c.1478C>G	ENSP00000489636.1:p.Pro493Arg
ENST00000637904.1:c.1637C>G	ENSP00000490550.1:p.Pro546Arg
ENST00000647938.1:c.3767C>G	ENSP00000498155.1:p.Pro1256Arg
ENST00000346085.9:c.3767C>G	ENSP00000344546.4:p.Pro1256Arg
ENST00000350026.9:c.3728C>G	ENSP00000055163.7:p.Pro1243Arg
ENST00000414678.6:c.2294C>G	ENSP00000412835.2:p.Pro765Arg
NM_017519.2:c.3728C>G	NP_059989.2:p.Pro1243Arg
NM_020732.3:c.3767C>G	NP_065783.3:p.Pro1256Arg
XM_005267069.3:c.3887C>G	XP_005267126.2:p.Pro1296Arg
XM_011535984.1:c.2966C>G	XP_011534286.1:p.Pro989Arg
XM_011535985.1:c.2786C>G	XP_011534287.1:p.Pro929Arg
XM_011535986.1:c.2546C>G	XP_011534288.1:p.Pro849Arg
XM_011535987.1:c.2165C>G	XP_011534289.1:p.Pro722Arg
XM_011535988.1:c.1028C>G	XP_011534290.1:p.Pro343Arg
NM_001346813.1:c.3887C>G	NP_001333742.1:p.Pro1296Arg
NM_001363725.1:c.1637C>G	NP_001350654.1:p.Pro546Arg
XM_011535984.2:c.4097C>G	XP_011534286.2:p.Pro1366Arg
XM_011535988.3:c.1028C>G	XP_011534290.1:p.Pro343Arg
XM_017011103.2:c.3998C>G	XP_016866592.1:p.Pro1333Arg
XM_017011104.1:c.3968C>G	XP_016866593.1:p.Pro1323Arg
XM_017011105.2:c.3938C>G	XP_016866594.1:p.Pro1313Arg
XM_017011106.2:c.3809C>G	XP_016866595.1:p.Pro1270Arg
XM_017011107.2:c.3788C>G	XP_016866596.1:p.Pro1263Arg
XR_002956289.1:n.4180C>G
NM_001363725.2:c.1637C>G	NP_001350654.1:p.Pro546Arg
NM_001371656.1:c.4016C>G	NP_001358585.1:p.Pro1339Arg
NM_001374820.1:c.4016C>G	NP_001361749.1:p.Pro1339Arg
NM_001374828.1:c.4136C>G MANE Select	NP_001361757.1:p.Pro1379Arg
NM_017519.3:c.3977C>G	NP_059989.3:p.Pro1326Arg