Canonical Allele Identifier: CA1914327430

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963647_61963648delinsGC , CM000672.2:g.61963647_61963648delinsGC	GRCh38
NC_000010.10:g.63723406_63723407delinsGC , CM000672.1:g.63723406_63723407delinsGC	GRCh37
NC_000010.9:g.63393412_63393413delinsGC	NCBI36
NG_030027.1:g.67394_67395delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+23239_502+23240delinsGC MANE Select	ENSP00000279873.7:n.502+23239_502+23240delinsGC
ENST00000644638.1:c.502+23239_502+23240delinsGC	ENSP00000494412.1:n.502+23239_502+23240delinsGC
ENST00000681100.1:c.502+23239_502+23240delinsGC	ENSP00000506119.1:n.502+23239_502+23240delinsGC
ENST00000279873.11:c.502+23239_502+23240delinsGC	ENSP00000279873.7:n.502+23239_502+23240delinsGC
NM_032199.2:c.502+23239_502+23240delinsGC	NP_115575.1:n.502+23239_502+23240delinsGC
XM_011540262.1:c.502+23239_502+23240delinsGC	XP_011538564.1:n.502+23239_502+23240delinsGC
XM_024448230.1:c.-66+23239_-66+23240delinsGC	XP_024303998.1:n.-66+23239_-66+23240delinsGC
NM_032199.3:c.502+23239_502+23240delinsGC MANE Select	NP_115575.1:n.502+23239_502+23240delinsGC