Canonical Allele Identifier: CA1675538396
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190080T= , CM000668.2:g.157190080T= GRCh38
NC_000006.11:g.157511214T= , CM000668.1:g.157511214T= GRCh37
NC_000006.10:g.157552906T= NCBI36
NG_032093.1:g.417151T=
NG_032093.2:g.417151T=
NG_066624.1:g.419055T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3942T= ENSP00000055163.8:p.Ser1314=
ENST00000414678.8:c.4011T= ENSP00000412835.3:p.Ser1337=
ENST00000637015.2:c.4230T= ENSP00000489729.2:p.Ser1410=
ENST00000346085.10:c.3981T= ENSP00000344546.5:p.Ser1327=
ENST00000350026.10:c.3693T= ENSP00000055163.7:p.Ser1231=
ENST00000414678.7:c.2259T= ENSP00000412835.2:p.Ser753=
ENST00000635849.1:c.1422T= ENSP00000490948.1:p.Ser474=
ENST00000635957.1:c.1053T= ENSP00000490385.1:p.Ser351=
ENST00000636930.2:c.4101T= MANE Select ENSP00000490491.2:p.Ser1367=
ENST00000636940.1:n.2098T=
ENST00000637015.1:c.1469T=
ENST00000637568.1:c.1383T=
ENST00000637741.1:n.767T=
ENST00000637810.1:c.1443T= ENSP00000489636.1:p.Ser481=
ENST00000637904.1:c.1602T= ENSP00000490550.1:p.Ser534=
ENST00000647938.1:c.3732T= ENSP00000498155.1:p.Ser1244=
ENST00000346085.9:c.3732T= ENSP00000344546.4:p.Ser1244=
ENST00000350026.9:c.3693T= ENSP00000055163.7:p.Ser1231=
ENST00000414678.6:c.2259T= ENSP00000412835.2:p.Ser753=
NM_017519.2:c.3693T= NP_059989.2:p.Ser1231=
NM_020732.3:c.3732T= NP_065783.3:p.Ser1244=
XM_005267069.3:c.3852T= XP_005267126.2:p.Ser1284=
XM_011535984.1:c.2931T= XP_011534286.1:p.Ser977=
XM_011535985.1:c.2751T= XP_011534287.1:p.Ser917=
XM_011535986.1:c.2511T= XP_011534288.1:p.Ser837=
XM_011535987.1:c.2130T= XP_011534289.1:p.Ser710=
XM_011535988.1:c.993T= XP_011534290.1:p.Ser331=
NM_001346813.1:c.3852T= NP_001333742.1:p.Ser1284=
NM_001363725.1:c.1602T= NP_001350654.1:p.Ser534=
XM_011535984.2:c.4062T= XP_011534286.2:p.Ser1354=
XM_011535988.3:c.993T= XP_011534290.1:p.Ser331=
XM_017011103.2:c.3963T= XP_016866592.1:p.Ser1321=
XM_017011104.1:c.3933T= XP_016866593.1:p.Ser1311=
XM_017011105.2:c.3903T= XP_016866594.1:p.Ser1301=
XM_017011106.2:c.3774T= XP_016866595.1:p.Ser1258=
XM_017011107.2:c.3753T= XP_016866596.1:p.Ser1251=
XR_002956289.1:n.4145T=
NM_001363725.2:c.1602T= NP_001350654.1:p.Ser534=
NM_001371656.1:c.3981T= NP_001358585.1:p.Ser1327=
NM_001374820.1:c.3981T= NP_001361749.1:p.Ser1327=
NM_001374828.1:c.4101T= MANE Select NP_001361757.1:p.Ser1367=
NM_017519.3:c.3942T= NP_059989.3:p.Ser1314=