Canonical Allele Identifier: CA1914338164
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838868419

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61987868del , CM000672.2:g.61987868del GRCh38
NC_000010.10:g.63747627del , CM000672.1:g.63747627del GRCh37
NC_000010.9:g.63417633del NCBI36
NG_030027.1:g.91615del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-12223del MANE Select ENSP00000279873.7:n.503-12223del
ENST00000644638.1:c.503-12223del ENSP00000494412.1:n.503-12223del
ENST00000681100.1:c.503-12223del ENSP00000506119.1:n.503-12223del
ENST00000279873.11:c.503-12223del ENSP00000279873.7:n.503-12223del
NM_032199.2:c.503-12223del NP_115575.1:n.503-12223del
XM_011540262.1:c.502+47460del XP_011538564.1:n.502+47460del
XM_024448230.1:c.-65-12223del XP_024303998.1:n.-65-12223del
NM_032199.3:c.503-12223del MANE Select NP_115575.1:n.503-12223del