Canonical Allele Identifier: CA366235094

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3949T>G	ENSP00000055163.8:p.Ser1317Ala
ENST00000414678.8:c.4018T>G	ENSP00000412835.3:p.Ser1340Ala
ENST00000637015.2:c.4237T>G	ENSP00000489729.2:p.Ser1413Ala
ENST00000346085.10:c.3988T>G	ENSP00000344546.5:p.Ser1330Ala
ENST00000350026.10:c.3700T>G	ENSP00000055163.7:p.Ser1234Ala
ENST00000414678.7:c.2266T>G	ENSP00000412835.2:p.Ser756Ala
ENST00000635849.1:c.1429T>G	ENSP00000490948.1:p.Ser477Ala
ENST00000635957.1:c.1060T>G	ENSP00000490385.1:p.Ser354Ala
ENST00000636930.2:c.4108T>G MANE Select	ENSP00000490491.2:p.Ser1370Ala
ENST00000636940.1:n.2105T>G
ENST00000637015.1:c.1476T>G
ENST00000637568.1:c.1390T>G
ENST00000637741.1:n.774T>G
ENST00000637810.1:c.1450T>G	ENSP00000489636.1:p.Ser484Ala
ENST00000637904.1:c.1609T>G	ENSP00000490550.1:p.Ser537Ala
ENST00000647938.1:c.3739T>G	ENSP00000498155.1:p.Ser1247Ala
ENST00000346085.9:c.3739T>G	ENSP00000344546.4:p.Ser1247Ala
ENST00000350026.9:c.3700T>G	ENSP00000055163.7:p.Ser1234Ala
ENST00000414678.6:c.2266T>G	ENSP00000412835.2:p.Ser756Ala
NM_017519.2:c.3700T>G	NP_059989.2:p.Ser1234Ala
NM_020732.3:c.3739T>G	NP_065783.3:p.Ser1247Ala
XM_005267069.3:c.3859T>G	XP_005267126.2:p.Ser1287Ala
XM_011535984.1:c.2938T>G	XP_011534286.1:p.Ser980Ala
XM_011535985.1:c.2758T>G	XP_011534287.1:p.Ser920Ala
XM_011535986.1:c.2518T>G	XP_011534288.1:p.Ser840Ala
XM_011535987.1:c.2137T>G	XP_011534289.1:p.Ser713Ala
XM_011535988.1:c.1000T>G	XP_011534290.1:p.Ser334Ala
NM_001346813.1:c.3859T>G	NP_001333742.1:p.Ser1287Ala
NM_001363725.1:c.1609T>G	NP_001350654.1:p.Ser537Ala
XM_011535984.2:c.4069T>G	XP_011534286.2:p.Ser1357Ala
XM_011535988.3:c.1000T>G	XP_011534290.1:p.Ser334Ala
XM_017011103.2:c.3970T>G	XP_016866592.1:p.Ser1324Ala
XM_017011104.1:c.3940T>G	XP_016866593.1:p.Ser1314Ala
XM_017011105.2:c.3910T>G	XP_016866594.1:p.Ser1304Ala
XM_017011106.2:c.3781T>G	XP_016866595.1:p.Ser1261Ala
XM_017011107.2:c.3760T>G	XP_016866596.1:p.Ser1254Ala
XR_002956289.1:n.4152T>G
NM_001363725.2:c.1609T>G	NP_001350654.1:p.Ser537Ala
NM_001371656.1:c.3988T>G	NP_001358585.1:p.Ser1330Ala
NM_001374820.1:c.3988T>G	NP_001361749.1:p.Ser1330Ala
NM_001374828.1:c.4108T>G MANE Select	NP_001361757.1:p.Ser1370Ala
NM_017519.3:c.3949T>G	NP_059989.3:p.Ser1317Ala