Canonical Allele Identifier: CA366240734
Community Standard Title: NM_001374828.1(ARID1B):c.4509C>G (p.Tyr1503Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157200734C>G , CM000668.2:g.157200734C>G GRCh38
NC_000006.11:g.157521868C>G , CM000668.1:g.157521868C>G GRCh37
NC_000006.10:g.157563560C>G NCBI36
NG_032093.1:g.427805C>G
NG_032093.2:g.427805C>G
NG_066624.1:g.429709C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.4509C>G MANE Select NP_001361757.1:p.Tyr1503Ter
ENST00000636930.2:c.4509C>G MANE Select ENSP00000490491.2:p.Tyr1503Ter
NM_001346813.1:c.4260C>G NP_001333742.1:p.Tyr1420Ter
NM_001363725.1:c.2010C>G NP_001350654.1:p.Tyr670Ter
NM_001363725.2:c.2010C>G NP_001350654.1:p.Tyr670Ter
NM_001371656.1:c.4389C>G NP_001358585.1:p.Tyr1463Ter
NM_001374820.1:c.4389C>G NP_001361749.1:p.Tyr1463Ter
NM_017519.2:c.4101C>G NP_059989.2:p.Tyr1367Ter
NM_017519.3:c.4350C>G NP_059989.3:p.Tyr1450Ter
NM_020732.3:c.4140C>G NP_065783.3:p.Tyr1380Ter
ENST00000346085.10:c.4389C>G ENSP00000344546.5:p.Tyr1463Ter
ENST00000346085.9:c.4140C>G ENSP00000344546.4:p.Tyr1380Ter
ENST00000350026.10:c.4101C>G ENSP00000055163.7:p.Tyr1367Ter
ENST00000350026.11:c.4350C>G ENSP00000055163.8:p.Tyr1450Ter
ENST00000350026.9:c.4101C>G ENSP00000055163.7:p.Tyr1367Ter
ENST00000414678.6:c.2667C>G ENSP00000412835.2:p.Tyr889Ter
ENST00000414678.7:c.2667C>G ENSP00000412835.2:p.Tyr889Ter
ENST00000414678.8:c.4419C>G ENSP00000412835.3:p.Tyr1473Ter
ENST00000635849.1:c.1830C>G ENSP00000490948.1:p.Tyr610Ter
ENST00000635957.1:c.1461C>G ENSP00000490385.1:p.Tyr487Ter
ENST00000636227.1:n.2972C>G
ENST00000636254.1:n.429C>G
ENST00000636940.1:n.2506C>G
ENST00000637015.1:c.1877C>G
ENST00000637015.2:c.4638C>G ENSP00000489729.2:p.Tyr1546Ter
ENST00000637568.1:c.1791C>G
ENST00000637741.1:n.1175C>G
ENST00000637810.1:c.1851C>G ENSP00000489636.1:p.Tyr617Ter
ENST00000637904.1:c.2010C>G ENSP00000490550.1:p.Tyr670Ter
ENST00000647938.1:c.4140C>G ENSP00000498155.1:p.Tyr1380Ter
XM_005267069.3:c.4260C>G XP_005267126.2:p.Tyr1420Ter
XM_011535984.1:c.3339C>G XP_011534286.1:p.Tyr1113Ter
XM_011535984.2:c.4470C>G XP_011534286.2:p.Tyr1490Ter
XM_011535985.1:c.3159C>G XP_011534287.1:p.Tyr1053Ter
XM_011535986.1:c.2919C>G XP_011534288.1:p.Tyr973Ter
XM_011535987.1:c.2538C>G XP_011534289.1:p.Tyr846Ter
XM_011535988.1:c.1401C>G XP_011534290.1:p.Tyr467Ter
XM_011535988.3:c.1401C>G XP_011534290.1:p.Tyr467Ter
XM_017011103.2:c.4371C>G XP_016866592.1:p.Tyr1457Ter
XM_017011104.1:c.4341C>G XP_016866593.1:p.Tyr1447Ter
XM_017011105.2:c.4311C>G XP_016866594.1:p.Tyr1437Ter
XM_017011106.2:c.4182C>G XP_016866595.1:p.Tyr1394Ter
XM_017011107.2:c.4161C>G XP_016866596.1:p.Tyr1387Ter
XR_002956289.1:n.4456C>G