Canonical Allele Identifier: CA366234882

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511198C>A (hg19) ; chr6:g.157190064C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190064C>A , CM000668.2:g.157190064C>A	GRCh38
NC_000006.11:g.157511198C>A , CM000668.1:g.157511198C>A	GRCh37
NC_000006.10:g.157552890C>A	NCBI36
NG_032093.1:g.417135C>A
NG_032093.2:g.417135C>A
NG_066624.1:g.419039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3926C>A	ENSP00000055163.8:p.Pro1309Gln
ENST00000414678.8:c.3995C>A	ENSP00000412835.3:p.Pro1332Gln
ENST00000637015.2:c.4214C>A	ENSP00000489729.2:p.Pro1405Gln
ENST00000346085.10:c.3965C>A	ENSP00000344546.5:p.Pro1322Gln
ENST00000350026.10:c.3677C>A	ENSP00000055163.7:p.Pro1226Gln
ENST00000414678.7:c.2243C>A	ENSP00000412835.2:p.Pro748Gln
ENST00000635849.1:c.1406C>A	ENSP00000490948.1:p.Pro469Gln
ENST00000635957.1:c.1037C>A	ENSP00000490385.1:p.Pro346Gln
ENST00000636930.2:c.4085C>A MANE Select	ENSP00000490491.2:p.Pro1362Gln
ENST00000636940.1:n.2082C>A
ENST00000637015.1:c.1453C>A
ENST00000637568.1:c.1367C>A
ENST00000637741.1:n.751C>A
ENST00000637810.1:c.1427C>A	ENSP00000489636.1:p.Pro476Gln
ENST00000637904.1:c.1586C>A	ENSP00000490550.1:p.Pro529Gln
ENST00000647938.1:c.3716C>A	ENSP00000498155.1:p.Pro1239Gln
ENST00000346085.9:c.3716C>A	ENSP00000344546.4:p.Pro1239Gln
ENST00000350026.9:c.3677C>A	ENSP00000055163.7:p.Pro1226Gln
ENST00000414678.6:c.2243C>A	ENSP00000412835.2:p.Pro748Gln
NM_017519.2:c.3677C>A	NP_059989.2:p.Pro1226Gln
NM_020732.3:c.3716C>A	NP_065783.3:p.Pro1239Gln
XM_005267069.3:c.3836C>A	XP_005267126.2:p.Pro1279Gln
XM_011535984.1:c.2915C>A	XP_011534286.1:p.Pro972Gln
XM_011535985.1:c.2735C>A	XP_011534287.1:p.Pro912Gln
XM_011535986.1:c.2495C>A	XP_011534288.1:p.Pro832Gln
XM_011535987.1:c.2114C>A	XP_011534289.1:p.Pro705Gln
XM_011535988.1:c.977C>A	XP_011534290.1:p.Pro326Gln
NM_001346813.1:c.3836C>A	NP_001333742.1:p.Pro1279Gln
NM_001363725.1:c.1586C>A	NP_001350654.1:p.Pro529Gln
XM_011535984.2:c.4046C>A	XP_011534286.2:p.Pro1349Gln
XM_011535988.3:c.977C>A	XP_011534290.1:p.Pro326Gln
XM_017011103.2:c.3947C>A	XP_016866592.1:p.Pro1316Gln
XM_017011104.1:c.3917C>A	XP_016866593.1:p.Pro1306Gln
XM_017011105.2:c.3887C>A	XP_016866594.1:p.Pro1296Gln
XM_017011106.2:c.3758C>A	XP_016866595.1:p.Pro1253Gln
XM_017011107.2:c.3737C>A	XP_016866596.1:p.Pro1246Gln
XR_002956289.1:n.4129C>A
NM_001363725.2:c.1586C>A	NP_001350654.1:p.Pro529Gln
NM_001371656.1:c.3965C>A	NP_001358585.1:p.Pro1322Gln
NM_001374820.1:c.3965C>A	NP_001361749.1:p.Pro1322Gln
NM_001374828.1:c.4085C>A MANE Select	NP_001361757.1:p.Pro1362Gln
NM_017519.3:c.3926C>A	NP_059989.3:p.Pro1309Gln