Canonical Allele Identifier: CA366234893

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3926C>T	ENSP00000055163.8:p.Pro1309Leu
ENST00000414678.8:c.3995C>T	ENSP00000412835.3:p.Pro1332Leu
ENST00000637015.2:c.4214C>T	ENSP00000489729.2:p.Pro1405Leu
ENST00000346085.10:c.3965C>T	ENSP00000344546.5:p.Pro1322Leu
ENST00000350026.10:c.3677C>T	ENSP00000055163.7:p.Pro1226Leu
ENST00000414678.7:c.2243C>T	ENSP00000412835.2:p.Pro748Leu
ENST00000635849.1:c.1406C>T	ENSP00000490948.1:p.Pro469Leu
ENST00000635957.1:c.1037C>T	ENSP00000490385.1:p.Pro346Leu
ENST00000636930.2:c.4085C>T MANE Select	ENSP00000490491.2:p.Pro1362Leu
ENST00000636940.1:n.2082C>T
ENST00000637015.1:c.1453C>T
ENST00000637568.1:c.1367C>T
ENST00000637741.1:n.751C>T
ENST00000637810.1:c.1427C>T	ENSP00000489636.1:p.Pro476Leu
ENST00000637904.1:c.1586C>T	ENSP00000490550.1:p.Pro529Leu
ENST00000647938.1:c.3716C>T	ENSP00000498155.1:p.Pro1239Leu
ENST00000346085.9:c.3716C>T	ENSP00000344546.4:p.Pro1239Leu
ENST00000350026.9:c.3677C>T	ENSP00000055163.7:p.Pro1226Leu
ENST00000414678.6:c.2243C>T	ENSP00000412835.2:p.Pro748Leu
NM_017519.2:c.3677C>T	NP_059989.2:p.Pro1226Leu
NM_020732.3:c.3716C>T	NP_065783.3:p.Pro1239Leu
XM_005267069.3:c.3836C>T	XP_005267126.2:p.Pro1279Leu
XM_011535984.1:c.2915C>T	XP_011534286.1:p.Pro972Leu
XM_011535985.1:c.2735C>T	XP_011534287.1:p.Pro912Leu
XM_011535986.1:c.2495C>T	XP_011534288.1:p.Pro832Leu
XM_011535987.1:c.2114C>T	XP_011534289.1:p.Pro705Leu
XM_011535988.1:c.977C>T	XP_011534290.1:p.Pro326Leu
NM_001346813.1:c.3836C>T	NP_001333742.1:p.Pro1279Leu
NM_001363725.1:c.1586C>T	NP_001350654.1:p.Pro529Leu
XM_011535984.2:c.4046C>T	XP_011534286.2:p.Pro1349Leu
XM_011535988.3:c.977C>T	XP_011534290.1:p.Pro326Leu
XM_017011103.2:c.3947C>T	XP_016866592.1:p.Pro1316Leu
XM_017011104.1:c.3917C>T	XP_016866593.1:p.Pro1306Leu
XM_017011105.2:c.3887C>T	XP_016866594.1:p.Pro1296Leu
XM_017011106.2:c.3758C>T	XP_016866595.1:p.Pro1253Leu
XM_017011107.2:c.3737C>T	XP_016866596.1:p.Pro1246Leu
XR_002956289.1:n.4129C>T
NM_001363725.2:c.1586C>T	NP_001350654.1:p.Pro529Leu
NM_001371656.1:c.3965C>T	NP_001358585.1:p.Pro1322Leu
NM_001374820.1:c.3965C>T	NP_001361749.1:p.Pro1322Leu
NM_001374828.1:c.4085C>T MANE Select	NP_001361757.1:p.Pro1362Leu
NM_017519.3:c.3926C>T	NP_059989.3:p.Pro1309Leu