Canonical Allele Identifier: CA366230393
Community Standard Title: NM_001374828.1(ARID1B):c.3813C>G (p.Tyr1271Ter)
Gene: ARID1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157184329C>G , CM000668.2:g.157184329C>G GRCh38
NC_000006.11:g.157505463C>G , CM000668.1:g.157505463C>G GRCh37
NC_000006.10:g.157547155C>G NCBI36
NG_032093.1:g.411400C>G
NG_032093.2:g.411400C>G
NG_066624.1:g.413304C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001374828.1:c.3813C>G MANE Select NP_001361757.1:p.Tyr1271Ter
ENST00000636930.2:c.3813C>G MANE Select ENSP00000490491.2:p.Tyr1271Ter
NM_001346813.1:c.3564C>G NP_001333742.1:p.Tyr1188Ter
NM_001363725.1:c.1314C>G NP_001350654.1:p.Tyr438Ter
NM_001363725.2:c.1314C>G NP_001350654.1:p.Tyr438Ter
NM_001371656.1:c.3693C>G NP_001358585.1:p.Tyr1231Ter
NM_001374820.1:c.3693C>G NP_001361749.1:p.Tyr1231Ter
NM_017519.2:c.3405C>G NP_059989.2:p.Tyr1135Ter
NM_017519.3:c.3654C>G NP_059989.3:p.Tyr1218Ter
NM_020732.3:c.3444C>G NP_065783.3:p.Tyr1148Ter
ENST00000319584.10:c.1830C>G ENSP00000313006.6:p.Tyr610Ter
ENST00000319584.11:c.1827C>G ENSP00000313006.7:p.Tyr609Ter
ENST00000346085.10:c.3693C>G ENSP00000344546.5:p.Tyr1231Ter
ENST00000346085.9:c.3444C>G ENSP00000344546.4:p.Tyr1148Ter
ENST00000350026.10:c.3405C>G ENSP00000055163.7:p.Tyr1135Ter
ENST00000350026.11:c.3654C>G ENSP00000055163.8:p.Tyr1218Ter
ENST00000350026.9:c.3405C>G ENSP00000055163.7:p.Tyr1135Ter
ENST00000400790.3:c.606C>G ENSP00000383596.3:p.Tyr202Ter
ENST00000414678.6:c.1971C>G ENSP00000412835.2:p.Tyr657Ter
ENST00000414678.7:c.1971C>G ENSP00000412835.2:p.Tyr657Ter
ENST00000414678.8:c.3723C>G ENSP00000412835.3:p.Tyr1241Ter
ENST00000635849.1:c.1134C>G ENSP00000490948.1:p.Tyr378Ter
ENST00000635957.1:c.768C>G ENSP00000490385.1:p.Tyr256Ter
ENST00000636940.1:n.1810C>G
ENST00000637015.1:c.1181C>G
ENST00000637015.2:c.3942C>G ENSP00000489729.2:p.Tyr1314Ter
ENST00000637568.1:c.1095C>G
ENST00000637741.1:n.479C>G
ENST00000637810.1:c.1155C>G ENSP00000489636.1:p.Tyr385Ter
ENST00000637904.1:c.1314C>G ENSP00000490550.1:p.Tyr438Ter
ENST00000647938.1:c.3444C>G ENSP00000498155.1:p.Tyr1148Ter
XM_005267069.3:c.3564C>G XP_005267126.2:p.Tyr1188Ter
XM_011535984.1:c.2643C>G XP_011534286.1:p.Tyr881Ter
XM_011535984.2:c.3774C>G XP_011534286.2:p.Tyr1258Ter
XM_011535985.1:c.2463C>G XP_011534287.1:p.Tyr821Ter
XM_011535986.1:c.2223C>G XP_011534288.1:p.Tyr741Ter
XM_011535987.1:c.1842C>G XP_011534289.1:p.Tyr614Ter
XM_011535988.1:c.705C>G XP_011534290.1:p.Tyr235Ter
XM_011535988.3:c.705C>G XP_011534290.1:p.Tyr235Ter
XM_017011103.2:c.3675C>G XP_016866592.1:p.Tyr1225Ter
XM_017011104.1:c.3645C>G XP_016866593.1:p.Tyr1215Ter
XM_017011105.2:c.3615C>G XP_016866594.1:p.Tyr1205Ter
XM_017011106.2:c.3486C>G XP_016866595.1:p.Tyr1162Ter
XM_017011107.2:c.3465C>G XP_016866596.1:p.Tyr1155Ter
XR_002956289.1:n.3857C>G