Canonical Allele Identifier: CA366249299
Community Standard Title: NM_001374828.1(ARID1B):c.6895C>T (p.Gln2299Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157207667C>T , CM000668.2:g.157207667C>T GRCh38
NC_000006.11:g.157528801C>T , CM000668.1:g.157528801C>T GRCh37
NC_000006.10:g.157570493C>T NCBI36
NG_032093.1:g.434738C>T
NG_032093.2:g.434738C>T
NG_066624.1:g.436642C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.6895C>T MANE Select NP_001361757.1:p.Gln2299Ter
ENST00000636930.2:c.6895C>T MANE Select ENSP00000490491.2:p.Gln2299Ter
NM_001346813.1:c.6646C>T NP_001333742.1:p.Gln2216Ter
NM_001363725.1:c.4396C>T NP_001350654.1:p.Gln1466Ter
NM_001363725.2:c.4396C>T NP_001350654.1:p.Gln1466Ter
NM_001371656.1:c.6775C>T NP_001358585.1:p.Gln2259Ter
NM_001374820.1:c.6775C>T NP_001361749.1:p.Gln2259Ter
NM_017519.2:c.6487C>T NP_059989.2:p.Gln2163Ter
NM_017519.3:c.6736C>T NP_059989.3:p.Gln2246Ter
NM_020732.3:c.6526C>T NP_065783.3:p.Gln2176Ter
ENST00000346085.10:c.6775C>T ENSP00000344546.5:p.Gln2259Ter
ENST00000346085.9:c.6526C>T ENSP00000344546.4:p.Gln2176Ter
ENST00000350026.10:c.6487C>T ENSP00000055163.7:p.Gln2163Ter
ENST00000350026.11:c.6736C>T ENSP00000055163.8:p.Gln2246Ter
ENST00000350026.9:c.6487C>T ENSP00000055163.7:p.Gln2163Ter
ENST00000414678.6:c.5053C>T ENSP00000412835.2:p.Gln1685Ter
ENST00000414678.7:c.5053C>T ENSP00000412835.2:p.Gln1685Ter
ENST00000414678.8:c.6805C>T ENSP00000412835.3:p.Gln2269Ter
ENST00000635849.1:c.4216C>T ENSP00000490948.1:p.Gln1406Ter
ENST00000635928.1:c.875+176C>T ENSP00000489717.1:n.875+176C>T
ENST00000635957.1:c.3847C>T ENSP00000490385.1:p.Gln1283Ter
ENST00000636227.1:n.5358C>T
ENST00000636254.1:n.2815C>T
ENST00000636940.1:n.4892C>T
ENST00000637015.1:c.4263C>T
ENST00000637015.2:c.7024C>T ENSP00000489729.2:p.Gln2342Ter
ENST00000637568.1:c.4177C>T
ENST00000637741.1:n.3561C>T
ENST00000637810.1:c.4237C>T ENSP00000489636.1:p.Gln1413Ter
ENST00000637904.1:c.4396C>T ENSP00000490550.1:p.Gln1466Ter
ENST00000637933.1:n.4010C>T
ENST00000647938.1:c.6526C>T ENSP00000498155.1:p.Gln2176Ter
XM_005267069.3:c.6646C>T XP_005267126.2:p.Gln2216Ter
XM_011535984.1:c.5725C>T XP_011534286.1:p.Gln1909Ter
XM_011535984.2:c.6856C>T XP_011534286.2:p.Gln2286Ter
XM_011535985.1:c.5545C>T XP_011534287.1:p.Gln1849Ter
XM_011535986.1:c.5305C>T XP_011534288.1:p.Gln1769Ter
XM_011535987.1:c.4924C>T XP_011534289.1:p.Gln1642Ter
XM_011535988.1:c.3787C>T XP_011534290.1:p.Gln1263Ter
XM_011535988.3:c.3787C>T XP_011534290.1:p.Gln1263Ter
XM_017011103.2:c.6757C>T XP_016866592.1:p.Gln2253Ter
XM_017011104.1:c.6727C>T XP_016866593.1:p.Gln2243Ter
XM_017011105.2:c.6697C>T XP_016866594.1:p.Gln2233Ter
XM_017011106.2:c.6568C>T XP_016866595.1:p.Gln2190Ter
XM_017011107.2:c.6547C>T XP_016866596.1:p.Gln2183Ter
XR_002956289.1:n.6842C>T