Canonical Allele Identifier: CA366235107

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3950C>G	ENSP00000055163.8:p.Ser1317Cys
ENST00000414678.8:c.4019C>G	ENSP00000412835.3:p.Ser1340Cys
ENST00000637015.2:c.4238C>G	ENSP00000489729.2:p.Ser1413Cys
ENST00000346085.10:c.3989C>G	ENSP00000344546.5:p.Ser1330Cys
ENST00000350026.10:c.3701C>G	ENSP00000055163.7:p.Ser1234Cys
ENST00000414678.7:c.2267C>G	ENSP00000412835.2:p.Ser756Cys
ENST00000635849.1:c.1430C>G	ENSP00000490948.1:p.Ser477Cys
ENST00000635957.1:c.1061C>G	ENSP00000490385.1:p.Ser354Cys
ENST00000636930.2:c.4109C>G MANE Select	ENSP00000490491.2:p.Ser1370Cys
ENST00000636940.1:n.2106C>G
ENST00000637015.1:c.1477C>G
ENST00000637568.1:c.1391C>G
ENST00000637741.1:n.775C>G
ENST00000637810.1:c.1451C>G	ENSP00000489636.1:p.Ser484Cys
ENST00000637904.1:c.1610C>G	ENSP00000490550.1:p.Ser537Cys
ENST00000647938.1:c.3740C>G	ENSP00000498155.1:p.Ser1247Cys
ENST00000346085.9:c.3740C>G	ENSP00000344546.4:p.Ser1247Cys
ENST00000350026.9:c.3701C>G	ENSP00000055163.7:p.Ser1234Cys
ENST00000414678.6:c.2267C>G	ENSP00000412835.2:p.Ser756Cys
NM_017519.2:c.3701C>G	NP_059989.2:p.Ser1234Cys
NM_020732.3:c.3740C>G	NP_065783.3:p.Ser1247Cys
XM_005267069.3:c.3860C>G	XP_005267126.2:p.Ser1287Cys
XM_011535984.1:c.2939C>G	XP_011534286.1:p.Ser980Cys
XM_011535985.1:c.2759C>G	XP_011534287.1:p.Ser920Cys
XM_011535986.1:c.2519C>G	XP_011534288.1:p.Ser840Cys
XM_011535987.1:c.2138C>G	XP_011534289.1:p.Ser713Cys
XM_011535988.1:c.1001C>G	XP_011534290.1:p.Ser334Cys
NM_001346813.1:c.3860C>G	NP_001333742.1:p.Ser1287Cys
NM_001363725.1:c.1610C>G	NP_001350654.1:p.Ser537Cys
XM_011535984.2:c.4070C>G	XP_011534286.2:p.Ser1357Cys
XM_011535988.3:c.1001C>G	XP_011534290.1:p.Ser334Cys
XM_017011103.2:c.3971C>G	XP_016866592.1:p.Ser1324Cys
XM_017011104.1:c.3941C>G	XP_016866593.1:p.Ser1314Cys
XM_017011105.2:c.3911C>G	XP_016866594.1:p.Ser1304Cys
XM_017011106.2:c.3782C>G	XP_016866595.1:p.Ser1261Cys
XM_017011107.2:c.3761C>G	XP_016866596.1:p.Ser1254Cys
XR_002956289.1:n.4153C>G
NM_001363725.2:c.1610C>G	NP_001350654.1:p.Ser537Cys
NM_001371656.1:c.3989C>G	NP_001358585.1:p.Ser1330Cys
NM_001374820.1:c.3989C>G	NP_001361749.1:p.Ser1330Cys
NM_001374828.1:c.4109C>G MANE Select	NP_001361757.1:p.Ser1370Cys
NM_017519.3:c.3950C>G	NP_059989.3:p.Ser1317Cys