Canonical Allele Identifier: CA366242532

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522457T>G (hg19) ; chr6:g.157201323T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201323T>G , CM000668.2:g.157201323T>G	GRCh38
NC_000006.11:g.157522457T>G , CM000668.1:g.157522457T>G	GRCh37
NC_000006.10:g.157564149T>G	NCBI36
NG_032093.1:g.428394T>G
NG_032093.2:g.428394T>G
NG_066624.1:g.430298T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4939T>G	ENSP00000055163.8:p.Ser1647Ala
ENST00000414678.8:c.5008T>G	ENSP00000412835.3:p.Ser1670Ala
ENST00000637015.2:c.5227T>G	ENSP00000489729.2:p.Ser1743Ala
ENST00000346085.10:c.4978T>G	ENSP00000344546.5:p.Ser1660Ala
ENST00000350026.10:c.4690T>G	ENSP00000055163.7:p.Ser1564Ala
ENST00000414678.7:c.3256T>G	ENSP00000412835.2:p.Ser1086Ala
ENST00000635849.1:c.2419T>G	ENSP00000490948.1:p.Ser807Ala
ENST00000635957.1:c.2050T>G	ENSP00000490385.1:p.Ser684Ala
ENST00000636227.1:n.3561T>G
ENST00000636254.1:n.1018T>G
ENST00000636930.2:c.5098T>G MANE Select	ENSP00000490491.2:p.Ser1700Ala
ENST00000636940.1:n.3095T>G
ENST00000637015.1:c.2466T>G
ENST00000637568.1:c.2380T>G
ENST00000637741.1:n.1764T>G
ENST00000637810.1:c.2440T>G	ENSP00000489636.1:p.Ser814Ala
ENST00000637904.1:c.2599T>G	ENSP00000490550.1:p.Ser867Ala
ENST00000647938.1:c.4729T>G	ENSP00000498155.1:p.Ser1577Ala
ENST00000346085.9:c.4729T>G	ENSP00000344546.4:p.Ser1577Ala
ENST00000350026.9:c.4690T>G	ENSP00000055163.7:p.Ser1564Ala
ENST00000414678.6:c.3256T>G	ENSP00000412835.2:p.Ser1086Ala
NM_017519.2:c.4690T>G	NP_059989.2:p.Ser1564Ala
NM_020732.3:c.4729T>G	NP_065783.3:p.Ser1577Ala
XM_005267069.3:c.4849T>G	XP_005267126.2:p.Ser1617Ala
XM_011535984.1:c.3928T>G	XP_011534286.1:p.Ser1310Ala
XM_011535985.1:c.3748T>G	XP_011534287.1:p.Ser1250Ala
XM_011535986.1:c.3508T>G	XP_011534288.1:p.Ser1170Ala
XM_011535987.1:c.3127T>G	XP_011534289.1:p.Ser1043Ala
XM_011535988.1:c.1990T>G	XP_011534290.1:p.Ser664Ala
NM_001346813.1:c.4849T>G	NP_001333742.1:p.Ser1617Ala
NM_001363725.1:c.2599T>G	NP_001350654.1:p.Ser867Ala
XM_011535984.2:c.5059T>G	XP_011534286.2:p.Ser1687Ala
XM_011535988.3:c.1990T>G	XP_011534290.1:p.Ser664Ala
XM_017011103.2:c.4960T>G	XP_016866592.1:p.Ser1654Ala
XM_017011104.1:c.4930T>G	XP_016866593.1:p.Ser1644Ala
XM_017011105.2:c.4900T>G	XP_016866594.1:p.Ser1634Ala
XM_017011106.2:c.4771T>G	XP_016866595.1:p.Ser1591Ala
XM_017011107.2:c.4750T>G	XP_016866596.1:p.Ser1584Ala
XR_002956289.1:n.5045T>G
NM_001363725.2:c.2599T>G	NP_001350654.1:p.Ser867Ala
NM_001371656.1:c.4978T>G	NP_001358585.1:p.Ser1660Ala
NM_001374820.1:c.4978T>G	NP_001361749.1:p.Ser1660Ala
NM_001374828.1:c.5098T>G MANE Select	NP_001361757.1:p.Ser1700Ala
NM_017519.3:c.4939T>G	NP_059989.3:p.Ser1647Ala