Canonical Allele Identifier: CA366247749
Community Standard Title: NM_001374828.1(ARID1B):c.6199C>T (p.Arg2067Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157206971C>T , CM000668.2:g.157206971C>T GRCh38
NC_000006.11:g.157528105C>T , CM000668.1:g.157528105C>T GRCh37
NC_000006.10:g.157569797C>T NCBI36
NG_032093.1:g.434042C>T
NG_032093.2:g.434042C>T
NG_066624.1:g.435946C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.6199C>T MANE Select NP_001361757.1:p.Arg2067Ter
ENST00000636930.2:c.6199C>T MANE Select ENSP00000490491.2:p.Arg2067Ter
NM_001346813.1:c.5950C>T NP_001333742.1:p.Arg1984Ter
NM_001363725.1:c.3700C>T NP_001350654.1:p.Arg1234Ter
NM_001363725.2:c.3700C>T NP_001350654.1:p.Arg1234Ter
NM_001371656.1:c.6079C>T NP_001358585.1:p.Arg2027Ter
NM_001374820.1:c.6079C>T NP_001361749.1:p.Arg2027Ter
NM_017519.2:c.5791C>T NP_059989.2:p.Arg1931Ter
NM_017519.3:c.6040C>T NP_059989.3:p.Arg2014Ter
NM_020732.3:c.5830C>T NP_065783.3:p.Arg1944Ter
ENST00000346085.10:c.6079C>T ENSP00000344546.5:p.Arg2027Ter
ENST00000346085.9:c.5830C>T ENSP00000344546.4:p.Arg1944Ter
ENST00000350026.10:c.5791C>T ENSP00000055163.7:p.Arg1931Ter
ENST00000350026.11:c.6040C>T ENSP00000055163.8:p.Arg2014Ter
ENST00000350026.9:c.5791C>T ENSP00000055163.7:p.Arg1931Ter
ENST00000414678.6:c.4357C>T ENSP00000412835.2:p.Arg1453Ter
ENST00000414678.7:c.4357C>T ENSP00000412835.2:p.Arg1453Ter
ENST00000414678.8:c.6109C>T ENSP00000412835.3:p.Arg2037Ter
ENST00000635849.1:c.3520C>T ENSP00000490948.1:p.Arg1174Ter
ENST00000635928.1:c.355C>T ENSP00000489717.1:p.Arg119Ter
ENST00000635957.1:c.3151C>T ENSP00000490385.1:p.Arg1051Ter
ENST00000636227.1:n.4662C>T
ENST00000636254.1:n.2119C>T
ENST00000636940.1:n.4196C>T
ENST00000637015.1:c.3567C>T
ENST00000637015.2:c.6328C>T ENSP00000489729.2:p.Arg2110Ter
ENST00000637568.1:c.3481C>T
ENST00000637741.1:n.2865C>T
ENST00000637810.1:c.3541C>T ENSP00000489636.1:p.Arg1181Ter
ENST00000637904.1:c.3700C>T ENSP00000490550.1:p.Arg1234Ter
ENST00000637933.1:n.3314C>T
ENST00000647938.1:c.5830C>T ENSP00000498155.1:p.Arg1944Ter
XM_005267069.3:c.5950C>T XP_005267126.2:p.Arg1984Ter
XM_011535984.1:c.5029C>T XP_011534286.1:p.Arg1677Ter
XM_011535984.2:c.6160C>T XP_011534286.2:p.Arg2054Ter
XM_011535985.1:c.4849C>T XP_011534287.1:p.Arg1617Ter
XM_011535986.1:c.4609C>T XP_011534288.1:p.Arg1537Ter
XM_011535987.1:c.4228C>T XP_011534289.1:p.Arg1410Ter
XM_011535988.1:c.3091C>T XP_011534290.1:p.Arg1031Ter
XM_011535988.3:c.3091C>T XP_011534290.1:p.Arg1031Ter
XM_017011103.2:c.6061C>T XP_016866592.1:p.Arg2021Ter
XM_017011104.1:c.6031C>T XP_016866593.1:p.Arg2011Ter
XM_017011105.2:c.6001C>T XP_016866594.1:p.Arg2001Ter
XM_017011106.2:c.5872C>T XP_016866595.1:p.Arg1958Ter
XM_017011107.2:c.5851C>T XP_016866596.1:p.Arg1951Ter
XR_002956289.1:n.6146C>T