Canonical Allele Identifier: CA366235309
Gene: ARID1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157190119C>A , CM000668.2:g.157190119C>A GRCh38
NC_000006.11:g.157511253C>A , CM000668.1:g.157511253C>A GRCh37
NC_000006.10:g.157552945C>A NCBI36
NG_032093.1:g.417190C>A
NG_032093.2:g.417190C>A
NG_066624.1:g.419094C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.3981C>A ENSP00000055163.8:p.Asn1327Lys
ENST00000414678.8:c.4050C>A ENSP00000412835.3:p.Asn1350Lys
ENST00000637015.2:c.4269C>A ENSP00000489729.2:p.Asn1423Lys
ENST00000346085.10:c.4020C>A ENSP00000344546.5:p.Asn1340Lys
ENST00000350026.10:c.3732C>A ENSP00000055163.7:p.Asn1244Lys
ENST00000414678.7:c.2298C>A ENSP00000412835.2:p.Asn766Lys
ENST00000635849.1:c.1461C>A ENSP00000490948.1:p.Asn487Lys
ENST00000635957.1:c.1092C>A ENSP00000490385.1:p.Asn364Lys
ENST00000636930.2:c.4140C>A MANE Select ENSP00000490491.2:p.Asn1380Lys
ENST00000636940.1:n.2137C>A
ENST00000637015.1:c.1508C>A
ENST00000637568.1:c.1422C>A
ENST00000637741.1:n.806C>A
ENST00000637810.1:c.1482C>A ENSP00000489636.1:p.Asn494Lys
ENST00000637904.1:c.1641C>A ENSP00000490550.1:p.Asn547Lys
ENST00000647938.1:c.3771C>A ENSP00000498155.1:p.Asn1257Lys
ENST00000346085.9:c.3771C>A ENSP00000344546.4:p.Asn1257Lys
ENST00000350026.9:c.3732C>A ENSP00000055163.7:p.Asn1244Lys
ENST00000414678.6:c.2298C>A ENSP00000412835.2:p.Asn766Lys
NM_017519.2:c.3732C>A NP_059989.2:p.Asn1244Lys
NM_020732.3:c.3771C>A NP_065783.3:p.Asn1257Lys
XM_005267069.3:c.3891C>A XP_005267126.2:p.Asn1297Lys
XM_011535984.1:c.2970C>A XP_011534286.1:p.Asn990Lys
XM_011535985.1:c.2790C>A XP_011534287.1:p.Asn930Lys
XM_011535986.1:c.2550C>A XP_011534288.1:p.Asn850Lys
XM_011535987.1:c.2169C>A XP_011534289.1:p.Asn723Lys
XM_011535988.1:c.1032C>A XP_011534290.1:p.Asn344Lys
NM_001346813.1:c.3891C>A NP_001333742.1:p.Asn1297Lys
NM_001363725.1:c.1641C>A NP_001350654.1:p.Asn547Lys
XM_011535984.2:c.4101C>A XP_011534286.2:p.Asn1367Lys
XM_011535988.3:c.1032C>A XP_011534290.1:p.Asn344Lys
XM_017011103.2:c.4002C>A XP_016866592.1:p.Asn1334Lys
XM_017011104.1:c.3972C>A XP_016866593.1:p.Asn1324Lys
XM_017011105.2:c.3942C>A XP_016866594.1:p.Asn1314Lys
XM_017011106.2:c.3813C>A XP_016866595.1:p.Asn1271Lys
XM_017011107.2:c.3792C>A XP_016866596.1:p.Asn1264Lys
XR_002956289.1:n.4184C>A
NM_001363725.2:c.1641C>A NP_001350654.1:p.Asn547Lys
NM_001371656.1:c.4020C>A NP_001358585.1:p.Asn1340Lys
NM_001374820.1:c.4020C>A NP_001361749.1:p.Asn1340Lys
NM_001374828.1:c.4140C>A MANE Select NP_001361757.1:p.Asn1380Lys
NM_017519.3:c.3981C>A NP_059989.3:p.Asn1327Lys