Canonical Allele Identifier: CA1096292567
Gene: ARID1B HGNC NCBI

Linked Data

dbSNP Id: rs1789966380

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148549_157148551del , CM000668.2:g.157148549_157148551del GRCh38
NC_000006.11:g.157469683_157469685del , CM000668.1:g.157469683_157469685del GRCh37
NC_000006.10:g.157511375_157511377del NCBI36
NG_032093.1:g.375620_375622del
NG_032093.2:g.375620_375622del
NG_066624.1:g.377524_377526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.2762-75_2762-73del ENSP00000055163.8:n.2762-75_2762-73del
ENST00000414678.8:c.2672-75_2672-73del ENSP00000412835.3:n.2672-75_2672-73del
ENST00000637015.2:c.2762-75_2762-73del ENSP00000489729.2:n.2762-75_2762-73del
ENST00000319584.11:c.776-75_776-73del ENSP00000313006.7:n.776-75_776-73del
ENST00000346085.10:c.2801-75_2801-73del ENSP00000344546.5:n.2801-75_2801-73del
ENST00000350026.10:c.2513-75_2513-73del ENSP00000055163.7:n.2513-75_2513-73del
ENST00000414678.7:c.920-75_920-73del ENSP00000412835.2:n.920-75_920-73del
ENST00000452544.2:n.663-75_663-73del
ENST00000635849.1:c.83-75_83-73del ENSP00000490948.1:n.83-75_83-73del
ENST00000636930.2:c.2762-75_2762-73del MANE Select ENSP00000490491.2:n.2762-75_2762-73del
ENST00000637810.1:c.263-75_263-73del ENSP00000489636.1:n.263-75_263-73del
ENST00000637904.1:c.263-75_263-73del ENSP00000490550.1:n.263-75_263-73del
ENST00000647938.1:c.2552-75_2552-73del ENSP00000498155.1:n.2552-75_2552-73del
ENST00000674190.1:n.1511-75_1511-73del
ENST00000319584.10:c.779-75_779-73del ENSP00000313006.6:n.779-75_779-73del
ENST00000346085.9:c.2552-75_2552-73del ENSP00000344546.4:n.2552-75_2552-73del
ENST00000350026.9:c.2513-75_2513-73del ENSP00000055163.7:n.2513-75_2513-73del
ENST00000414678.6:c.920-75_920-73del ENSP00000412835.2:n.920-75_920-73del
ENST00000452544.1:n.609-75_609-73del
NM_017519.2:c.2513-75_2513-73del NP_059989.2:n.2513-75_2513-73del
NM_020732.3:c.2552-75_2552-73del NP_065783.3:n.2552-75_2552-73del
XM_005267069.3:c.2513-75_2513-73del XP_005267126.2:n.2513-75_2513-73del
XM_011535984.1:c.1463-75_1463-73del XP_011534286.1:n.1463-75_1463-73del
XM_011535985.1:c.1283-75_1283-73del XP_011534287.1:n.1283-75_1283-73del
XM_011535986.1:c.1043-75_1043-73del XP_011534288.1:n.1043-75_1043-73del
XM_011535987.1:c.662-75_662-73del XP_011534289.1:n.662-75_662-73del
XM_011535988.1:c.-20+15342_-20+15344del XP_011534290.1:n.-20+15342_-20+15344del
NM_001346813.1:c.2513-75_2513-73del NP_001333742.1:n.2513-75_2513-73del
NM_001363725.1:c.263-75_263-73del NP_001350654.1:n.263-75_263-73del
XM_011535984.2:c.2594-75_2594-73del XP_011534286.2:n.2594-75_2594-73del
XM_011535988.3:c.-20+15342_-20+15344del XP_011534290.1:n.-20+15342_-20+15344del
XM_017011103.2:c.2594-75_2594-73del XP_016866592.1:n.2594-75_2594-73del
XM_017011104.1:c.2594-75_2594-73del XP_016866593.1:n.2594-75_2594-73del
XM_017011105.2:c.2594-75_2594-73del XP_016866594.1:n.2594-75_2594-73del
XM_017011106.2:c.2594-75_2594-73del XP_016866595.1:n.2594-75_2594-73del
XM_017011107.2:c.2414-75_2414-73del XP_016866596.1:n.2414-75_2414-73del
XR_002956289.1:n.2677-75_2677-73del
NM_001363725.2:c.263-75_263-73del NP_001350654.1:n.263-75_263-73del
NM_001371656.1:c.2801-75_2801-73del NP_001358585.1:n.2801-75_2801-73del
NM_001374820.1:c.2801-75_2801-73del NP_001361749.1:n.2801-75_2801-73del
NM_001374828.1:c.2762-75_2762-73del MANE Select NP_001361757.1:n.2762-75_2762-73del
NM_017519.3:c.2762-75_2762-73del NP_059989.3:n.2762-75_2762-73del