Canonical Allele Identifier: CA1914314660
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1844277276

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61935145del , CM000672.2:g.61935145del GRCh38
NC_000010.10:g.63694904del , CM000672.1:g.63694904del GRCh37
NC_000010.9:g.63364910del NCBI36
NG_030027.1:g.38892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.277-5038del MANE Select ENSP00000279873.7:n.277-5038del
ENST00000644638.1:c.277-5038del ENSP00000494412.1:n.277-5038del
ENST00000681100.1:c.277-5038del ENSP00000506119.1:n.277-5038del
ENST00000279873.11:c.277-5038del ENSP00000279873.7:n.277-5038del
NM_032199.2:c.277-5038del NP_115575.1:n.277-5038del
XM_011540262.1:c.277-5038del XP_011538564.1:n.277-5038del
XM_024448230.1:c.-291-5038del XP_024303998.1:n.-291-5038del
NM_032199.3:c.277-5038del MANE Select NP_115575.1:n.277-5038del