Canonical Allele Identifier: CA366249263
Community Standard Title: NM_001374828.1(ARID1B):c.6880C>T (p.Gln2294Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157207652C>T , CM000668.2:g.157207652C>T GRCh38
NC_000006.11:g.157528786C>T , CM000668.1:g.157528786C>T GRCh37
NC_000006.10:g.157570478C>T NCBI36
NG_032093.1:g.434723C>T
NG_032093.2:g.434723C>T
NG_066624.1:g.436627C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.6880C>T MANE Select NP_001361757.1:p.Gln2294Ter
ENST00000636930.2:c.6880C>T MANE Select ENSP00000490491.2:p.Gln2294Ter
NM_001346813.1:c.6631C>T NP_001333742.1:p.Gln2211Ter
NM_001363725.1:c.4381C>T NP_001350654.1:p.Gln1461Ter
NM_001363725.2:c.4381C>T NP_001350654.1:p.Gln1461Ter
NM_001371656.1:c.6760C>T NP_001358585.1:p.Gln2254Ter
NM_001374820.1:c.6760C>T NP_001361749.1:p.Gln2254Ter
NM_017519.2:c.6472C>T NP_059989.2:p.Gln2158Ter
NM_017519.3:c.6721C>T NP_059989.3:p.Gln2241Ter
NM_020732.3:c.6511C>T NP_065783.3:p.Gln2171Ter
ENST00000346085.10:c.6760C>T ENSP00000344546.5:p.Gln2254Ter
ENST00000346085.9:c.6511C>T ENSP00000344546.4:p.Gln2171Ter
ENST00000350026.10:c.6472C>T ENSP00000055163.7:p.Gln2158Ter
ENST00000350026.11:c.6721C>T ENSP00000055163.8:p.Gln2241Ter
ENST00000350026.9:c.6472C>T ENSP00000055163.7:p.Gln2158Ter
ENST00000414678.6:c.5038C>T ENSP00000412835.2:p.Gln1680Ter
ENST00000414678.7:c.5038C>T ENSP00000412835.2:p.Gln1680Ter
ENST00000414678.8:c.6790C>T ENSP00000412835.3:p.Gln2264Ter
ENST00000635849.1:c.4201C>T ENSP00000490948.1:p.Gln1401Ter
ENST00000635928.1:c.875+161C>T ENSP00000489717.1:n.875+161C>T
ENST00000635957.1:c.3832C>T ENSP00000490385.1:p.Gln1278Ter
ENST00000636227.1:n.5343C>T
ENST00000636254.1:n.2800C>T
ENST00000636940.1:n.4877C>T
ENST00000637015.1:c.4248C>T
ENST00000637015.2:c.7009C>T ENSP00000489729.2:p.Gln2337Ter
ENST00000637568.1:c.4162C>T
ENST00000637741.1:n.3546C>T
ENST00000637810.1:c.4222C>T ENSP00000489636.1:p.Gln1408Ter
ENST00000637904.1:c.4381C>T ENSP00000490550.1:p.Gln1461Ter
ENST00000637933.1:n.3995C>T
ENST00000647938.1:c.6511C>T ENSP00000498155.1:p.Gln2171Ter
XM_005267069.3:c.6631C>T XP_005267126.2:p.Gln2211Ter
XM_011535984.1:c.5710C>T XP_011534286.1:p.Gln1904Ter
XM_011535984.2:c.6841C>T XP_011534286.2:p.Gln2281Ter
XM_011535985.1:c.5530C>T XP_011534287.1:p.Gln1844Ter
XM_011535986.1:c.5290C>T XP_011534288.1:p.Gln1764Ter
XM_011535987.1:c.4909C>T XP_011534289.1:p.Gln1637Ter
XM_011535988.1:c.3772C>T XP_011534290.1:p.Gln1258Ter
XM_011535988.3:c.3772C>T XP_011534290.1:p.Gln1258Ter
XM_017011103.2:c.6742C>T XP_016866592.1:p.Gln2248Ter
XM_017011104.1:c.6712C>T XP_016866593.1:p.Gln2238Ter
XM_017011105.2:c.6682C>T XP_016866594.1:p.Gln2228Ter
XM_017011106.2:c.6553C>T XP_016866595.1:p.Gln2185Ter
XM_017011107.2:c.6532C>T XP_016866596.1:p.Gln2178Ter
XR_002956289.1:n.6827C>T