Canonical Allele Identifier: CA366242048

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522256A>G (hg19) ; chr6:g.157201122A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201122A>G , CM000668.2:g.157201122A>G	GRCh38
NC_000006.11:g.157522256A>G , CM000668.1:g.157522256A>G	GRCh37
NC_000006.10:g.157563948A>G	NCBI36
NG_032093.1:g.428193A>G
NG_032093.2:g.428193A>G
NG_066624.1:g.430097A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4738A>G	ENSP00000055163.8:p.Ser1580Gly
ENST00000414678.8:c.4807A>G	ENSP00000412835.3:p.Ser1603Gly
ENST00000637015.2:c.5026A>G	ENSP00000489729.2:p.Ser1676Gly
ENST00000346085.10:c.4777A>G	ENSP00000344546.5:p.Ser1593Gly
ENST00000350026.10:c.4489A>G	ENSP00000055163.7:p.Ser1497Gly
ENST00000414678.7:c.3055A>G	ENSP00000412835.2:p.Ser1019Gly
ENST00000635849.1:c.2218A>G	ENSP00000490948.1:p.Ser740Gly
ENST00000635957.1:c.1849A>G	ENSP00000490385.1:p.Ser617Gly
ENST00000636227.1:n.3360A>G
ENST00000636254.1:n.817A>G
ENST00000636930.2:c.4897A>G MANE Select	ENSP00000490491.2:p.Ser1633Gly
ENST00000636940.1:n.2894A>G
ENST00000637015.1:c.2265A>G
ENST00000637568.1:c.2179A>G
ENST00000637741.1:n.1563A>G
ENST00000637810.1:c.2239A>G	ENSP00000489636.1:p.Ser747Gly
ENST00000637904.1:c.2398A>G	ENSP00000490550.1:p.Ser800Gly
ENST00000647938.1:c.4528A>G	ENSP00000498155.1:p.Ser1510Gly
ENST00000346085.9:c.4528A>G	ENSP00000344546.4:p.Ser1510Gly
ENST00000350026.9:c.4489A>G	ENSP00000055163.7:p.Ser1497Gly
ENST00000414678.6:c.3055A>G	ENSP00000412835.2:p.Ser1019Gly
NM_017519.2:c.4489A>G	NP_059989.2:p.Ser1497Gly
NM_020732.3:c.4528A>G	NP_065783.3:p.Ser1510Gly
XM_005267069.3:c.4648A>G	XP_005267126.2:p.Ser1550Gly
XM_011535984.1:c.3727A>G	XP_011534286.1:p.Ser1243Gly
XM_011535985.1:c.3547A>G	XP_011534287.1:p.Ser1183Gly
XM_011535986.1:c.3307A>G	XP_011534288.1:p.Ser1103Gly
XM_011535987.1:c.2926A>G	XP_011534289.1:p.Ser976Gly
XM_011535988.1:c.1789A>G	XP_011534290.1:p.Ser597Gly
NM_001346813.1:c.4648A>G	NP_001333742.1:p.Ser1550Gly
NM_001363725.1:c.2398A>G	NP_001350654.1:p.Ser800Gly
XM_011535984.2:c.4858A>G	XP_011534286.2:p.Ser1620Gly
XM_011535988.3:c.1789A>G	XP_011534290.1:p.Ser597Gly
XM_017011103.2:c.4759A>G	XP_016866592.1:p.Ser1587Gly
XM_017011104.1:c.4729A>G	XP_016866593.1:p.Ser1577Gly
XM_017011105.2:c.4699A>G	XP_016866594.1:p.Ser1567Gly
XM_017011106.2:c.4570A>G	XP_016866595.1:p.Ser1524Gly
XM_017011107.2:c.4549A>G	XP_016866596.1:p.Ser1517Gly
XR_002956289.1:n.4844A>G
NM_001363725.2:c.2398A>G	NP_001350654.1:p.Ser800Gly
NM_001371656.1:c.4777A>G	NP_001358585.1:p.Ser1593Gly
NM_001374820.1:c.4777A>G	NP_001361749.1:p.Ser1593Gly
NM_001374828.1:c.4897A>G MANE Select	NP_001361757.1:p.Ser1633Gly
NM_017519.3:c.4738A>G	NP_059989.3:p.Ser1580Gly