Canonical Allele Identifier: CA366248978
Community Standard Title: NM_001374828.1(ARID1B):c.6751C>T (p.Arg2251Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157207523C>T , CM000668.2:g.157207523C>T GRCh38
NC_000006.11:g.157528657C>T , CM000668.1:g.157528657C>T GRCh37
NC_000006.10:g.157570349C>T NCBI36
NG_032093.1:g.434594C>T
NG_032093.2:g.434594C>T
NG_066624.1:g.436498C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.6751C>T MANE Select NP_001361757.1:p.Arg2251Ter
ENST00000636930.2:c.6751C>T MANE Select ENSP00000490491.2:p.Arg2251Ter
NM_001346813.1:c.6502C>T NP_001333742.1:p.Arg2168Ter
NM_001363725.1:c.4252C>T NP_001350654.1:p.Arg1418Ter
NM_001363725.2:c.4252C>T NP_001350654.1:p.Arg1418Ter
NM_001371656.1:c.6631C>T NP_001358585.1:p.Arg2211Ter
NM_001374820.1:c.6631C>T NP_001361749.1:p.Arg2211Ter
NM_017519.2:c.6343C>T NP_059989.2:p.Arg2115Ter
NM_017519.3:c.6592C>T NP_059989.3:p.Arg2198Ter
NM_020732.3:c.6382C>T NP_065783.3:p.Arg2128Ter
ENST00000346085.10:c.6631C>T ENSP00000344546.5:p.Arg2211Ter
ENST00000346085.9:c.6382C>T ENSP00000344546.4:p.Arg2128Ter
ENST00000350026.10:c.6343C>T ENSP00000055163.7:p.Arg2115Ter
ENST00000350026.11:c.6592C>T ENSP00000055163.8:p.Arg2198Ter
ENST00000350026.9:c.6343C>T ENSP00000055163.7:p.Arg2115Ter
ENST00000414678.6:c.4909C>T ENSP00000412835.2:p.Arg1637Ter
ENST00000414678.7:c.4909C>T ENSP00000412835.2:p.Arg1637Ter
ENST00000414678.8:c.6661C>T ENSP00000412835.3:p.Arg2221Ter
ENST00000635849.1:c.4072C>T ENSP00000490948.1:p.Arg1358Ter
ENST00000635928.1:c.875+32C>T ENSP00000489717.1:n.875+32C>T
ENST00000635957.1:c.3703C>T ENSP00000490385.1:p.Arg1235Ter
ENST00000636227.1:n.5214C>T
ENST00000636254.1:n.2671C>T
ENST00000636940.1:n.4748C>T
ENST00000637015.1:c.4119C>T
ENST00000637015.2:c.6880C>T ENSP00000489729.2:p.Arg2294Ter
ENST00000637568.1:c.4033C>T
ENST00000637741.1:n.3417C>T
ENST00000637810.1:c.4093C>T ENSP00000489636.1:p.Arg1365Ter
ENST00000637904.1:c.4252C>T ENSP00000490550.1:p.Arg1418Ter
ENST00000637933.1:n.3866C>T
ENST00000647938.1:c.6382C>T ENSP00000498155.1:p.Arg2128Ter
XM_005267069.3:c.6502C>T XP_005267126.2:p.Arg2168Ter
XM_011535984.1:c.5581C>T XP_011534286.1:p.Arg1861Ter
XM_011535984.2:c.6712C>T XP_011534286.2:p.Arg2238Ter
XM_011535985.1:c.5401C>T XP_011534287.1:p.Arg1801Ter
XM_011535986.1:c.5161C>T XP_011534288.1:p.Arg1721Ter
XM_011535987.1:c.4780C>T XP_011534289.1:p.Arg1594Ter
XM_011535988.1:c.3643C>T XP_011534290.1:p.Arg1215Ter
XM_011535988.3:c.3643C>T XP_011534290.1:p.Arg1215Ter
XM_017011103.2:c.6613C>T XP_016866592.1:p.Arg2205Ter
XM_017011104.1:c.6583C>T XP_016866593.1:p.Arg2195Ter
XM_017011105.2:c.6553C>T XP_016866594.1:p.Arg2185Ter
XM_017011106.2:c.6424C>T XP_016866595.1:p.Arg2142Ter
XM_017011107.2:c.6403C>T XP_016866596.1:p.Arg2135Ter
XR_002956289.1:n.6698C>T