Canonical Allele Identifier: CA366230809
Community Standard Title: NM_001374828.1(ARID1B):c.3904C>T (p.Gln1302Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184420C>T , CM000668.2:g.157184420C>T GRCh38
NC_000006.11:g.157505554C>T , CM000668.1:g.157505554C>T GRCh37
NC_000006.10:g.157547246C>T NCBI36
NG_032093.1:g.411491C>T
NG_032093.2:g.411491C>T
NG_066624.1:g.413395C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.3904C>T MANE Select NP_001361757.1:p.Gln1302Ter
ENST00000636930.2:c.3904C>T MANE Select ENSP00000490491.2:p.Gln1302Ter
NM_001346813.1:c.3655C>T NP_001333742.1:p.Gln1219Ter
NM_001363725.1:c.1405C>T NP_001350654.1:p.Gln469Ter
NM_001363725.2:c.1405C>T NP_001350654.1:p.Gln469Ter
NM_001371656.1:c.3784C>T NP_001358585.1:p.Gln1262Ter
NM_001374820.1:c.3784C>T NP_001361749.1:p.Gln1262Ter
NM_017519.2:c.3496C>T NP_059989.2:p.Gln1166Ter
NM_017519.3:c.3745C>T NP_059989.3:p.Gln1249Ter
NM_020732.3:c.3535C>T NP_065783.3:p.Gln1179Ter
ENST00000319584.10:c.1921C>T ENSP00000313006.6:p.Gln641Ter
ENST00000319584.11:c.1918C>T ENSP00000313006.7:p.Gln640Ter
ENST00000346085.10:c.3784C>T ENSP00000344546.5:p.Gln1262Ter
ENST00000346085.9:c.3535C>T ENSP00000344546.4:p.Gln1179Ter
ENST00000350026.10:c.3496C>T ENSP00000055163.7:p.Gln1166Ter
ENST00000350026.11:c.3745C>T ENSP00000055163.8:p.Gln1249Ter
ENST00000350026.9:c.3496C>T ENSP00000055163.7:p.Gln1166Ter
ENST00000400790.3:c.697C>T ENSP00000383596.3:p.Gln233Ter
ENST00000414678.6:c.2062C>T ENSP00000412835.2:p.Gln688Ter
ENST00000414678.7:c.2062C>T ENSP00000412835.2:p.Gln688Ter
ENST00000414678.8:c.3814C>T ENSP00000412835.3:p.Gln1272Ter
ENST00000635849.1:c.1225C>T ENSP00000490948.1:p.Gln409Ter
ENST00000635957.1:c.859C>T ENSP00000490385.1:p.Gln287Ter
ENST00000636940.1:n.1901C>T
ENST00000637015.1:c.1272C>T
ENST00000637015.2:c.4033C>T ENSP00000489729.2:p.Gln1345Ter
ENST00000637568.1:c.1186C>T
ENST00000637741.1:n.570C>T
ENST00000637810.1:c.1246C>T ENSP00000489636.1:p.Gln416Ter
ENST00000637904.1:c.1405C>T ENSP00000490550.1:p.Gln469Ter
ENST00000647938.1:c.3535C>T ENSP00000498155.1:p.Gln1179Ter
XM_005267069.3:c.3655C>T XP_005267126.2:p.Gln1219Ter
XM_011535984.1:c.2734C>T XP_011534286.1:p.Gln912Ter
XM_011535984.2:c.3865C>T XP_011534286.2:p.Gln1289Ter
XM_011535985.1:c.2554C>T XP_011534287.1:p.Gln852Ter
XM_011535986.1:c.2314C>T XP_011534288.1:p.Gln772Ter
XM_011535987.1:c.1933C>T XP_011534289.1:p.Gln645Ter
XM_011535988.1:c.796C>T XP_011534290.1:p.Gln266Ter
XM_011535988.3:c.796C>T XP_011534290.1:p.Gln266Ter
XM_017011103.2:c.3766C>T XP_016866592.1:p.Gln1256Ter
XM_017011104.1:c.3736C>T XP_016866593.1:p.Gln1246Ter
XM_017011105.2:c.3706C>T XP_016866594.1:p.Gln1236Ter
XM_017011106.2:c.3577C>T XP_016866595.1:p.Gln1193Ter
XM_017011107.2:c.3556C>T XP_016866596.1:p.Gln1186Ter
XR_002956289.1:n.3948C>T