Canonical Allele Identifier: CA1914327444
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838504500

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61963671del , CM000672.2:g.61963671del GRCh38
NC_000010.10:g.63723430del , CM000672.1:g.63723430del GRCh37
NC_000010.9:g.63393436del NCBI36
NG_030027.1:g.67418del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.502+23263del MANE Select ENSP00000279873.7:n.502+23263del
ENST00000644638.1:c.502+23263del ENSP00000494412.1:n.502+23263del
ENST00000681100.1:c.502+23263del ENSP00000506119.1:n.502+23263del
ENST00000279873.11:c.502+23263del ENSP00000279873.7:n.502+23263del
NM_032199.2:c.502+23263del NP_115575.1:n.502+23263del
XM_011540262.1:c.502+23263del XP_011538564.1:n.502+23263del
XM_024448230.1:c.-66+23263del XP_024303998.1:n.-66+23263del
NM_032199.3:c.502+23263del MANE Select NP_115575.1:n.502+23263del