Canonical Allele Identifier: CA2547376311
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61961325_61961326del , CM000672.2:g.61961325_61961326del GRCh38
NC_000010.10:g.63721084_63721085del , CM000672.1:g.63721084_63721085del GRCh37
NC_000010.9:g.63391090_63391091del NCBI36
NG_030027.1:g.65072_65073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.502+20917_502+20918del MANE Select ENSP00000279873.7:n.502+20917_502+20918del
ENST00000644638.1:c.502+20917_502+20918del ENSP00000494412.1:n.502+20917_502+20918del
ENST00000681100.1:c.502+20917_502+20918del ENSP00000506119.1:n.502+20917_502+20918del
ENST00000279873.11:c.502+20917_502+20918del ENSP00000279873.7:n.502+20917_502+20918del
NM_032199.2:c.502+20917_502+20918del NP_115575.1:n.502+20917_502+20918del
XM_011540262.1:c.502+20917_502+20918del XP_011538564.1:n.502+20917_502+20918del
XM_024448230.1:c.-66+20917_-66+20918del XP_024303998.1:n.-66+20917_-66+20918del
NM_032199.3:c.502+20917_502+20918del MANE Select NP_115575.1:n.502+20917_502+20918del