Canonical Allele Identifier: CA366242528

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375913
• MyVariant Identifiers: chr6:g.157522457T>A (hg19) ; chr6:g.157201323T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4939T>A	ENSP00000055163.8:p.Ser1647Thr
ENST00000414678.8:c.5008T>A	ENSP00000412835.3:p.Ser1670Thr
ENST00000637015.2:c.5227T>A	ENSP00000489729.2:p.Ser1743Thr
ENST00000346085.10:c.4978T>A	ENSP00000344546.5:p.Ser1660Thr
ENST00000350026.10:c.4690T>A	ENSP00000055163.7:p.Ser1564Thr
ENST00000414678.7:c.3256T>A	ENSP00000412835.2:p.Ser1086Thr
ENST00000635849.1:c.2419T>A	ENSP00000490948.1:p.Ser807Thr
ENST00000635957.1:c.2050T>A	ENSP00000490385.1:p.Ser684Thr
ENST00000636227.1:n.3561T>A
ENST00000636254.1:n.1018T>A
ENST00000636930.2:c.5098T>A MANE Select	ENSP00000490491.2:p.Ser1700Thr
ENST00000636940.1:n.3095T>A
ENST00000637015.1:c.2466T>A
ENST00000637568.1:c.2380T>A
ENST00000637741.1:n.1764T>A
ENST00000637810.1:c.2440T>A	ENSP00000489636.1:p.Ser814Thr
ENST00000637904.1:c.2599T>A	ENSP00000490550.1:p.Ser867Thr
ENST00000647938.1:c.4729T>A	ENSP00000498155.1:p.Ser1577Thr
ENST00000346085.9:c.4729T>A	ENSP00000344546.4:p.Ser1577Thr
ENST00000350026.9:c.4690T>A	ENSP00000055163.7:p.Ser1564Thr
ENST00000414678.6:c.3256T>A	ENSP00000412835.2:p.Ser1086Thr
NM_017519.2:c.4690T>A	NP_059989.2:p.Ser1564Thr
NM_020732.3:c.4729T>A	NP_065783.3:p.Ser1577Thr
XM_005267069.3:c.4849T>A	XP_005267126.2:p.Ser1617Thr
XM_011535984.1:c.3928T>A	XP_011534286.1:p.Ser1310Thr
XM_011535985.1:c.3748T>A	XP_011534287.1:p.Ser1250Thr
XM_011535986.1:c.3508T>A	XP_011534288.1:p.Ser1170Thr
XM_011535987.1:c.3127T>A	XP_011534289.1:p.Ser1043Thr
XM_011535988.1:c.1990T>A	XP_011534290.1:p.Ser664Thr
NM_001346813.1:c.4849T>A	NP_001333742.1:p.Ser1617Thr
NM_001363725.1:c.2599T>A	NP_001350654.1:p.Ser867Thr
XM_011535984.2:c.5059T>A	XP_011534286.2:p.Ser1687Thr
XM_011535988.3:c.1990T>A	XP_011534290.1:p.Ser664Thr
XM_017011103.2:c.4960T>A	XP_016866592.1:p.Ser1654Thr
XM_017011104.1:c.4930T>A	XP_016866593.1:p.Ser1644Thr
XM_017011105.2:c.4900T>A	XP_016866594.1:p.Ser1634Thr
XM_017011106.2:c.4771T>A	XP_016866595.1:p.Ser1591Thr
XM_017011107.2:c.4750T>A	XP_016866596.1:p.Ser1584Thr
XR_002956289.1:n.5045T>A
NM_001363725.2:c.2599T>A	NP_001350654.1:p.Ser867Thr
NM_001371656.1:c.4978T>A	NP_001358585.1:p.Ser1660Thr
NM_001374820.1:c.4978T>A	NP_001361749.1:p.Ser1660Thr
NM_001374828.1:c.5098T>A MANE Select	NP_001361757.1:p.Ser1700Thr
NM_017519.3:c.4939T>A	NP_059989.3:p.Ser1647Thr