Canonical Allele Identifier: CA366235098

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511222C>A (hg19) ; chr6:g.157190088C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190088C>A , CM000668.2:g.157190088C>A	GRCh38
NC_000006.11:g.157511222C>A , CM000668.1:g.157511222C>A	GRCh37
NC_000006.10:g.157552914C>A	NCBI36
NG_032093.1:g.417159C>A
NG_032093.2:g.417159C>A
NG_066624.1:g.419063C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3950C>A	ENSP00000055163.8:p.Ser1317Tyr
ENST00000414678.8:c.4019C>A	ENSP00000412835.3:p.Ser1340Tyr
ENST00000637015.2:c.4238C>A	ENSP00000489729.2:p.Ser1413Tyr
ENST00000346085.10:c.3989C>A	ENSP00000344546.5:p.Ser1330Tyr
ENST00000350026.10:c.3701C>A	ENSP00000055163.7:p.Ser1234Tyr
ENST00000414678.7:c.2267C>A	ENSP00000412835.2:p.Ser756Tyr
ENST00000635849.1:c.1430C>A	ENSP00000490948.1:p.Ser477Tyr
ENST00000635957.1:c.1061C>A	ENSP00000490385.1:p.Ser354Tyr
ENST00000636930.2:c.4109C>A MANE Select	ENSP00000490491.2:p.Ser1370Tyr
ENST00000636940.1:n.2106C>A
ENST00000637015.1:c.1477C>A
ENST00000637568.1:c.1391C>A
ENST00000637741.1:n.775C>A
ENST00000637810.1:c.1451C>A	ENSP00000489636.1:p.Ser484Tyr
ENST00000637904.1:c.1610C>A	ENSP00000490550.1:p.Ser537Tyr
ENST00000647938.1:c.3740C>A	ENSP00000498155.1:p.Ser1247Tyr
ENST00000346085.9:c.3740C>A	ENSP00000344546.4:p.Ser1247Tyr
ENST00000350026.9:c.3701C>A	ENSP00000055163.7:p.Ser1234Tyr
ENST00000414678.6:c.2267C>A	ENSP00000412835.2:p.Ser756Tyr
NM_017519.2:c.3701C>A	NP_059989.2:p.Ser1234Tyr
NM_020732.3:c.3740C>A	NP_065783.3:p.Ser1247Tyr
XM_005267069.3:c.3860C>A	XP_005267126.2:p.Ser1287Tyr
XM_011535984.1:c.2939C>A	XP_011534286.1:p.Ser980Tyr
XM_011535985.1:c.2759C>A	XP_011534287.1:p.Ser920Tyr
XM_011535986.1:c.2519C>A	XP_011534288.1:p.Ser840Tyr
XM_011535987.1:c.2138C>A	XP_011534289.1:p.Ser713Tyr
XM_011535988.1:c.1001C>A	XP_011534290.1:p.Ser334Tyr
NM_001346813.1:c.3860C>A	NP_001333742.1:p.Ser1287Tyr
NM_001363725.1:c.1610C>A	NP_001350654.1:p.Ser537Tyr
XM_011535984.2:c.4070C>A	XP_011534286.2:p.Ser1357Tyr
XM_011535988.3:c.1001C>A	XP_011534290.1:p.Ser334Tyr
XM_017011103.2:c.3971C>A	XP_016866592.1:p.Ser1324Tyr
XM_017011104.1:c.3941C>A	XP_016866593.1:p.Ser1314Tyr
XM_017011105.2:c.3911C>A	XP_016866594.1:p.Ser1304Tyr
XM_017011106.2:c.3782C>A	XP_016866595.1:p.Ser1261Tyr
XM_017011107.2:c.3761C>A	XP_016866596.1:p.Ser1254Tyr
XR_002956289.1:n.4153C>A
NM_001363725.2:c.1610C>A	NP_001350654.1:p.Ser537Tyr
NM_001371656.1:c.3989C>A	NP_001358585.1:p.Ser1330Tyr
NM_001374820.1:c.3989C>A	NP_001361749.1:p.Ser1330Tyr
NM_001374828.1:c.4109C>A MANE Select	NP_001361757.1:p.Ser1370Tyr
NM_017519.3:c.3950C>A	NP_059989.3:p.Ser1317Tyr