Canonical Allele Identifier: CA366242317

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522377T>G (hg19) ; chr6:g.157201243T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201243T>G , CM000668.2:g.157201243T>G	GRCh38
NC_000006.11:g.157522377T>G , CM000668.1:g.157522377T>G	GRCh37
NC_000006.10:g.157564069T>G	NCBI36
NG_032093.1:g.428314T>G
NG_032093.2:g.428314T>G
NG_066624.1:g.430218T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4859T>G	ENSP00000055163.8:p.Ile1620Ser
ENST00000414678.8:c.4928T>G	ENSP00000412835.3:p.Ile1643Ser
ENST00000637015.2:c.5147T>G	ENSP00000489729.2:p.Ile1716Ser
ENST00000346085.10:c.4898T>G	ENSP00000344546.5:p.Ile1633Ser
ENST00000350026.10:c.4610T>G	ENSP00000055163.7:p.Ile1537Ser
ENST00000414678.7:c.3176T>G	ENSP00000412835.2:p.Ile1059Ser
ENST00000635849.1:c.2339T>G	ENSP00000490948.1:p.Ile780Ser
ENST00000635957.1:c.1970T>G	ENSP00000490385.1:p.Ile657Ser
ENST00000636227.1:n.3481T>G
ENST00000636254.1:n.938T>G
ENST00000636930.2:c.5018T>G MANE Select	ENSP00000490491.2:p.Ile1673Ser
ENST00000636940.1:n.3015T>G
ENST00000637015.1:c.2386T>G
ENST00000637568.1:c.2300T>G
ENST00000637741.1:n.1684T>G
ENST00000637810.1:c.2360T>G	ENSP00000489636.1:p.Ile787Ser
ENST00000637904.1:c.2519T>G	ENSP00000490550.1:p.Ile840Ser
ENST00000647938.1:c.4649T>G	ENSP00000498155.1:p.Ile1550Ser
ENST00000346085.9:c.4649T>G	ENSP00000344546.4:p.Ile1550Ser
ENST00000350026.9:c.4610T>G	ENSP00000055163.7:p.Ile1537Ser
ENST00000414678.6:c.3176T>G	ENSP00000412835.2:p.Ile1059Ser
NM_017519.2:c.4610T>G	NP_059989.2:p.Ile1537Ser
NM_020732.3:c.4649T>G	NP_065783.3:p.Ile1550Ser
XM_005267069.3:c.4769T>G	XP_005267126.2:p.Ile1590Ser
XM_011535984.1:c.3848T>G	XP_011534286.1:p.Ile1283Ser
XM_011535985.1:c.3668T>G	XP_011534287.1:p.Ile1223Ser
XM_011535986.1:c.3428T>G	XP_011534288.1:p.Ile1143Ser
XM_011535987.1:c.3047T>G	XP_011534289.1:p.Ile1016Ser
XM_011535988.1:c.1910T>G	XP_011534290.1:p.Ile637Ser
NM_001346813.1:c.4769T>G	NP_001333742.1:p.Ile1590Ser
NM_001363725.1:c.2519T>G	NP_001350654.1:p.Ile840Ser
XM_011535984.2:c.4979T>G	XP_011534286.2:p.Ile1660Ser
XM_011535988.3:c.1910T>G	XP_011534290.1:p.Ile637Ser
XM_017011103.2:c.4880T>G	XP_016866592.1:p.Ile1627Ser
XM_017011104.1:c.4850T>G	XP_016866593.1:p.Ile1617Ser
XM_017011105.2:c.4820T>G	XP_016866594.1:p.Ile1607Ser
XM_017011106.2:c.4691T>G	XP_016866595.1:p.Ile1564Ser
XM_017011107.2:c.4670T>G	XP_016866596.1:p.Ile1557Ser
XR_002956289.1:n.4965T>G
NM_001363725.2:c.2519T>G	NP_001350654.1:p.Ile840Ser
NM_001371656.1:c.4898T>G	NP_001358585.1:p.Ile1633Ser
NM_001374820.1:c.4898T>G	NP_001361749.1:p.Ile1633Ser
NM_001374828.1:c.5018T>G MANE Select	NP_001361757.1:p.Ile1673Ser
NM_017519.3:c.4859T>G	NP_059989.3:p.Ile1620Ser