Canonical Allele Identifier: CA366234889

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3926C>G	ENSP00000055163.8:p.Pro1309Arg
ENST00000414678.8:c.3995C>G	ENSP00000412835.3:p.Pro1332Arg
ENST00000637015.2:c.4214C>G	ENSP00000489729.2:p.Pro1405Arg
ENST00000346085.10:c.3965C>G	ENSP00000344546.5:p.Pro1322Arg
ENST00000350026.10:c.3677C>G	ENSP00000055163.7:p.Pro1226Arg
ENST00000414678.7:c.2243C>G	ENSP00000412835.2:p.Pro748Arg
ENST00000635849.1:c.1406C>G	ENSP00000490948.1:p.Pro469Arg
ENST00000635957.1:c.1037C>G	ENSP00000490385.1:p.Pro346Arg
ENST00000636930.2:c.4085C>G MANE Select	ENSP00000490491.2:p.Pro1362Arg
ENST00000636940.1:n.2082C>G
ENST00000637015.1:c.1453C>G
ENST00000637568.1:c.1367C>G
ENST00000637741.1:n.751C>G
ENST00000637810.1:c.1427C>G	ENSP00000489636.1:p.Pro476Arg
ENST00000637904.1:c.1586C>G	ENSP00000490550.1:p.Pro529Arg
ENST00000647938.1:c.3716C>G	ENSP00000498155.1:p.Pro1239Arg
ENST00000346085.9:c.3716C>G	ENSP00000344546.4:p.Pro1239Arg
ENST00000350026.9:c.3677C>G	ENSP00000055163.7:p.Pro1226Arg
ENST00000414678.6:c.2243C>G	ENSP00000412835.2:p.Pro748Arg
NM_017519.2:c.3677C>G	NP_059989.2:p.Pro1226Arg
NM_020732.3:c.3716C>G	NP_065783.3:p.Pro1239Arg
XM_005267069.3:c.3836C>G	XP_005267126.2:p.Pro1279Arg
XM_011535984.1:c.2915C>G	XP_011534286.1:p.Pro972Arg
XM_011535985.1:c.2735C>G	XP_011534287.1:p.Pro912Arg
XM_011535986.1:c.2495C>G	XP_011534288.1:p.Pro832Arg
XM_011535987.1:c.2114C>G	XP_011534289.1:p.Pro705Arg
XM_011535988.1:c.977C>G	XP_011534290.1:p.Pro326Arg
NM_001346813.1:c.3836C>G	NP_001333742.1:p.Pro1279Arg
NM_001363725.1:c.1586C>G	NP_001350654.1:p.Pro529Arg
XM_011535984.2:c.4046C>G	XP_011534286.2:p.Pro1349Arg
XM_011535988.3:c.977C>G	XP_011534290.1:p.Pro326Arg
XM_017011103.2:c.3947C>G	XP_016866592.1:p.Pro1316Arg
XM_017011104.1:c.3917C>G	XP_016866593.1:p.Pro1306Arg
XM_017011105.2:c.3887C>G	XP_016866594.1:p.Pro1296Arg
XM_017011106.2:c.3758C>G	XP_016866595.1:p.Pro1253Arg
XM_017011107.2:c.3737C>G	XP_016866596.1:p.Pro1246Arg
XR_002956289.1:n.4129C>G
NM_001363725.2:c.1586C>G	NP_001350654.1:p.Pro529Arg
NM_001371656.1:c.3965C>G	NP_001358585.1:p.Pro1322Arg
NM_001374820.1:c.3965C>G	NP_001361749.1:p.Pro1322Arg
NM_001374828.1:c.4085C>G MANE Select	NP_001361757.1:p.Pro1362Arg
NM_017519.3:c.3926C>G	NP_059989.3:p.Pro1309Arg