Canonical Allele Identifier: CA366388616
Gene: ARID1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148630A>T , CM000668.2:g.157148630A>T GRCh38
NC_000006.11:g.157469764A>T , CM000668.1:g.157469764A>T GRCh37
NC_000006.10:g.157511456A>T NCBI36
NG_032093.1:g.375701A>T
NG_032093.2:g.375701A>T
NG_066624.1:g.377605A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.2768A>T ENSP00000055163.8:p.Tyr923Phe
ENST00000414678.8:c.2678A>T ENSP00000412835.3:p.Tyr893Phe
ENST00000637015.2:c.2768A>T ENSP00000489729.2:p.Tyr923Phe
ENST00000319584.11:c.782A>T ENSP00000313006.7:p.Tyr261Phe
ENST00000346085.10:c.2807A>T ENSP00000344546.5:p.Tyr936Phe
ENST00000350026.10:c.2519A>T ENSP00000055163.7:p.Tyr840Phe
ENST00000414678.7:c.926A>T ENSP00000412835.2:p.Tyr309Phe
ENST00000452544.2:n.669A>T
ENST00000635849.1:c.89A>T ENSP00000490948.1:p.Tyr30Phe
ENST00000636930.2:c.2768A>T MANE Select ENSP00000490491.2:p.Tyr923Phe
ENST00000637015.1:c.7A>T
ENST00000637810.1:c.269A>T ENSP00000489636.1:p.Tyr90Phe
ENST00000637904.1:c.269A>T ENSP00000490550.1:p.Tyr90Phe
ENST00000647938.1:c.2558A>T ENSP00000498155.1:p.Tyr853Phe
ENST00000674190.1:n.1517A>T
ENST00000319584.10:c.785A>T ENSP00000313006.6:p.Tyr262Phe
ENST00000346085.9:c.2558A>T ENSP00000344546.4:p.Tyr853Phe
ENST00000350026.9:c.2519A>T ENSP00000055163.7:p.Tyr840Phe
ENST00000414678.6:c.926A>T ENSP00000412835.2:p.Tyr309Phe
ENST00000452544.1:n.615A>T
NM_017519.2:c.2519A>T NP_059989.2:p.Tyr840Phe
NM_020732.3:c.2558A>T NP_065783.3:p.Tyr853Phe
XM_005267069.3:c.2519A>T XP_005267126.2:p.Tyr840Phe
XM_011535984.1:c.1469A>T XP_011534286.1:p.Tyr490Phe
XM_011535985.1:c.1289A>T XP_011534287.1:p.Tyr430Phe
XM_011535986.1:c.1049A>T XP_011534288.1:p.Tyr350Phe
XM_011535987.1:c.668A>T XP_011534289.1:p.Tyr223Phe
XM_011535988.1:c.-20+15423A>T XP_011534290.1:n.-20+15423A>T
NM_001346813.1:c.2519A>T NP_001333742.1:p.Tyr840Phe
NM_001363725.1:c.269A>T NP_001350654.1:p.Tyr90Phe
XM_011535984.2:c.2600A>T XP_011534286.2:p.Tyr867Phe
XM_011535988.3:c.-20+15423A>T XP_011534290.1:n.-20+15423A>T
XM_017011103.2:c.2600A>T XP_016866592.1:p.Tyr867Phe
XM_017011104.1:c.2600A>T XP_016866593.1:p.Tyr867Phe
XM_017011105.2:c.2600A>T XP_016866594.1:p.Tyr867Phe
XM_017011106.2:c.2600A>T XP_016866595.1:p.Tyr867Phe
XM_017011107.2:c.2420A>T XP_016866596.1:p.Tyr807Phe
XR_002956289.1:n.2683A>T
NM_001363725.2:c.269A>T NP_001350654.1:p.Tyr90Phe
NM_001371656.1:c.2807A>T NP_001358585.1:p.Tyr936Phe
NM_001374820.1:c.2807A>T NP_001361749.1:p.Tyr936Phe
NM_001374828.1:c.2768A>T MANE Select NP_001361757.1:p.Tyr923Phe
NM_017519.3:c.2768A>T NP_059989.3:p.Tyr923Phe