Canonical Allele Identifier: CA1675487200
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157084771C= , CM000668.2:g.157084771C= GRCh38
NC_000006.11:g.157405905C= , CM000668.1:g.157405905C= GRCh37
NC_000006.10:g.157447597C= NCBI36
NG_032093.1:g.311842C=
NG_032093.2:g.311842C=
NG_066624.1:g.313746C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.2357C= ENSP00000055163.8:p.Ala786=
ENST00000414678.8:c.2357C= ENSP00000412835.3:p.Ala786=
ENST00000637015.2:c.2357C= ENSP00000489729.2:p.Ala786=
ENST00000319584.11:c.371C= ENSP00000313006.7:p.Ala124=
ENST00000346085.10:c.2396C= ENSP00000344546.5:p.Ala799=
ENST00000350026.10:c.2108C= ENSP00000055163.7:p.Ala703=
ENST00000414678.7:c.605C= ENSP00000412835.2:p.Ala202=
ENST00000452544.2:n.258C=
ENST00000493658.2:n.6C=
ENST00000635849.1:c.-143C= ENSP00000490948.1:n.-143C=
ENST00000636930.2:c.2357C= MANE Select ENSP00000490491.2:p.Ala786=
ENST00000637003.1:c.-143C= ENSP00000489666.1:n.-143C=
ENST00000637904.1:c.-143C= ENSP00000490550.1:n.-143C=
ENST00000647938.1:c.2147C= ENSP00000498155.1:p.Ala716=
ENST00000674190.1:n.1106C=
ENST00000319584.10:c.374C= ENSP00000313006.6:p.Ala125=
ENST00000346085.9:c.2147C= ENSP00000344546.4:p.Ala716=
ENST00000350026.9:c.2108C= ENSP00000055163.7:p.Ala703=
ENST00000414678.6:c.605C= ENSP00000412835.2:p.Ala202=
ENST00000452544.1:n.216C=
ENST00000493658.1:n.6C=
NM_017519.2:c.2108C= NP_059989.2:p.Ala703=
NM_020732.3:c.2147C= NP_065783.3:p.Ala716=
XM_005267069.3:c.2108C= XP_005267126.2:p.Ala703=
XM_011535984.1:c.1058C= XP_011534286.1:p.Ala353=
XM_011535985.1:c.1058C= XP_011534287.1:p.Ala353=
XM_011535986.1:c.638C= XP_011534288.1:p.Ala213=
XM_011535987.1:c.257C= XP_011534289.1:p.Ala86=
NM_001346813.1:c.2108C= NP_001333742.1:p.Ala703=
NM_001363725.1:c.-143C= NP_001350654.1:n.-143C=
XM_011535984.2:c.2189C= XP_011534286.2:p.Ala730=
XM_017011103.2:c.2189C= XP_016866592.1:p.Ala730=
XM_017011104.1:c.2189C= XP_016866593.1:p.Ala730=
XM_017011105.2:c.2189C= XP_016866594.1:p.Ala730=
XM_017011106.2:c.2189C= XP_016866595.1:p.Ala730=
XM_017011107.2:c.2189C= XP_016866596.1:p.Ala730=
XR_002956289.1:n.2272C=
NM_001363725.2:c.-143C= NP_001350654.1:n.-143C=
NM_001371656.1:c.2396C= NP_001358585.1:p.Ala799=
NM_001374820.1:c.2396C= NP_001361749.1:p.Ala799=
NM_001374828.1:c.2357C= MANE Select NP_001361757.1:p.Ala786=
NM_017519.3:c.2357C= NP_059989.3:p.Ala786=