Canonical Allele Identifier: CA366230330
Community Standard Title: NM_001374828.1(ARID1B):c.3799C>T (p.Gln1267Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184315C>T , CM000668.2:g.157184315C>T GRCh38
NC_000006.11:g.157505449C>T , CM000668.1:g.157505449C>T GRCh37
NC_000006.10:g.157547141C>T NCBI36
NG_032093.1:g.411386C>T
NG_032093.2:g.411386C>T
NG_066624.1:g.413290C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.3799C>T MANE Select NP_001361757.1:p.Gln1267Ter
ENST00000636930.2:c.3799C>T MANE Select ENSP00000490491.2:p.Gln1267Ter
NM_001346813.1:c.3550C>T NP_001333742.1:p.Gln1184Ter
NM_001363725.1:c.1300C>T NP_001350654.1:p.Gln434Ter
NM_001363725.2:c.1300C>T NP_001350654.1:p.Gln434Ter
NM_001371656.1:c.3679C>T NP_001358585.1:p.Gln1227Ter
NM_001374820.1:c.3679C>T NP_001361749.1:p.Gln1227Ter
NM_017519.2:c.3391C>T NP_059989.2:p.Gln1131Ter
NM_017519.3:c.3640C>T NP_059989.3:p.Gln1214Ter
NM_020732.3:c.3430C>T NP_065783.3:p.Gln1144Ter
ENST00000319584.10:c.1816C>T ENSP00000313006.6:p.Gln606Ter
ENST00000319584.11:c.1813C>T ENSP00000313006.7:p.Gln605Ter
ENST00000346085.10:c.3679C>T ENSP00000344546.5:p.Gln1227Ter
ENST00000346085.9:c.3430C>T ENSP00000344546.4:p.Gln1144Ter
ENST00000350026.10:c.3391C>T ENSP00000055163.7:p.Gln1131Ter
ENST00000350026.11:c.3640C>T ENSP00000055163.8:p.Gln1214Ter
ENST00000350026.9:c.3391C>T ENSP00000055163.7:p.Gln1131Ter
ENST00000400790.3:c.592C>T ENSP00000383596.3:p.Gln198Ter
ENST00000414678.6:c.1957C>T ENSP00000412835.2:p.Gln653Ter
ENST00000414678.7:c.1957C>T ENSP00000412835.2:p.Gln653Ter
ENST00000414678.8:c.3709C>T ENSP00000412835.3:p.Gln1237Ter
ENST00000635849.1:c.1120C>T ENSP00000490948.1:p.Gln374Ter
ENST00000635957.1:c.754C>T ENSP00000490385.1:p.Gln252Ter
ENST00000636940.1:n.1796C>T
ENST00000637015.1:c.1167C>T
ENST00000637015.2:c.3928C>T ENSP00000489729.2:p.Gln1310Ter
ENST00000637568.1:c.1081C>T
ENST00000637741.1:n.465C>T
ENST00000637810.1:c.1141C>T ENSP00000489636.1:p.Gln381Ter
ENST00000637904.1:c.1300C>T ENSP00000490550.1:p.Gln434Ter
ENST00000647938.1:c.3430C>T ENSP00000498155.1:p.Gln1144Ter
XM_005267069.3:c.3550C>T XP_005267126.2:p.Gln1184Ter
XM_011535984.1:c.2629C>T XP_011534286.1:p.Gln877Ter
XM_011535984.2:c.3760C>T XP_011534286.2:p.Gln1254Ter
XM_011535985.1:c.2449C>T XP_011534287.1:p.Gln817Ter
XM_011535986.1:c.2209C>T XP_011534288.1:p.Gln737Ter
XM_011535987.1:c.1828C>T XP_011534289.1:p.Gln610Ter
XM_011535988.1:c.691C>T XP_011534290.1:p.Gln231Ter
XM_011535988.3:c.691C>T XP_011534290.1:p.Gln231Ter
XM_017011103.2:c.3661C>T XP_016866592.1:p.Gln1221Ter
XM_017011104.1:c.3631C>T XP_016866593.1:p.Gln1211Ter
XM_017011105.2:c.3601C>T XP_016866594.1:p.Gln1201Ter
XM_017011106.2:c.3472C>T XP_016866595.1:p.Gln1158Ter
XM_017011107.2:c.3451C>T XP_016866596.1:p.Gln1151Ter
XR_002956289.1:n.3843C>T