Canonical Allele Identifier: CA366235088

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511221T>A (hg19) ; chr6:g.157190087T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190087T>A , CM000668.2:g.157190087T>A	GRCh38
NC_000006.11:g.157511221T>A , CM000668.1:g.157511221T>A	GRCh37
NC_000006.10:g.157552913T>A	NCBI36
NG_032093.1:g.417158T>A
NG_032093.2:g.417158T>A
NG_066624.1:g.419062T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3949T>A	ENSP00000055163.8:p.Ser1317Thr
ENST00000414678.8:c.4018T>A	ENSP00000412835.3:p.Ser1340Thr
ENST00000637015.2:c.4237T>A	ENSP00000489729.2:p.Ser1413Thr
ENST00000346085.10:c.3988T>A	ENSP00000344546.5:p.Ser1330Thr
ENST00000350026.10:c.3700T>A	ENSP00000055163.7:p.Ser1234Thr
ENST00000414678.7:c.2266T>A	ENSP00000412835.2:p.Ser756Thr
ENST00000635849.1:c.1429T>A	ENSP00000490948.1:p.Ser477Thr
ENST00000635957.1:c.1060T>A	ENSP00000490385.1:p.Ser354Thr
ENST00000636930.2:c.4108T>A MANE Select	ENSP00000490491.2:p.Ser1370Thr
ENST00000636940.1:n.2105T>A
ENST00000637015.1:c.1476T>A
ENST00000637568.1:c.1390T>A
ENST00000637741.1:n.774T>A
ENST00000637810.1:c.1450T>A	ENSP00000489636.1:p.Ser484Thr
ENST00000637904.1:c.1609T>A	ENSP00000490550.1:p.Ser537Thr
ENST00000647938.1:c.3739T>A	ENSP00000498155.1:p.Ser1247Thr
ENST00000346085.9:c.3739T>A	ENSP00000344546.4:p.Ser1247Thr
ENST00000350026.9:c.3700T>A	ENSP00000055163.7:p.Ser1234Thr
ENST00000414678.6:c.2266T>A	ENSP00000412835.2:p.Ser756Thr
NM_017519.2:c.3700T>A	NP_059989.2:p.Ser1234Thr
NM_020732.3:c.3739T>A	NP_065783.3:p.Ser1247Thr
XM_005267069.3:c.3859T>A	XP_005267126.2:p.Ser1287Thr
XM_011535984.1:c.2938T>A	XP_011534286.1:p.Ser980Thr
XM_011535985.1:c.2758T>A	XP_011534287.1:p.Ser920Thr
XM_011535986.1:c.2518T>A	XP_011534288.1:p.Ser840Thr
XM_011535987.1:c.2137T>A	XP_011534289.1:p.Ser713Thr
XM_011535988.1:c.1000T>A	XP_011534290.1:p.Ser334Thr
NM_001346813.1:c.3859T>A	NP_001333742.1:p.Ser1287Thr
NM_001363725.1:c.1609T>A	NP_001350654.1:p.Ser537Thr
XM_011535984.2:c.4069T>A	XP_011534286.2:p.Ser1357Thr
XM_011535988.3:c.1000T>A	XP_011534290.1:p.Ser334Thr
XM_017011103.2:c.3970T>A	XP_016866592.1:p.Ser1324Thr
XM_017011104.1:c.3940T>A	XP_016866593.1:p.Ser1314Thr
XM_017011105.2:c.3910T>A	XP_016866594.1:p.Ser1304Thr
XM_017011106.2:c.3781T>A	XP_016866595.1:p.Ser1261Thr
XM_017011107.2:c.3760T>A	XP_016866596.1:p.Ser1254Thr
XR_002956289.1:n.4152T>A
NM_001363725.2:c.1609T>A	NP_001350654.1:p.Ser537Thr
NM_001371656.1:c.3988T>A	NP_001358585.1:p.Ser1330Thr
NM_001374820.1:c.3988T>A	NP_001361749.1:p.Ser1330Thr
NM_001374828.1:c.4108T>A MANE Select	NP_001361757.1:p.Ser1370Thr
NM_017519.3:c.3949T>A	NP_059989.3:p.Ser1317Thr