Canonical Allele Identifier: CA1914325242

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61958564_61958565delinsAT , CM000672.2:g.61958564_61958565delinsAT	GRCh38
NC_000010.10:g.63718323_63718324delinsAT , CM000672.1:g.63718323_63718324delinsAT	GRCh37
NC_000010.9:g.63388329_63388330delinsAT	NCBI36
NG_030027.1:g.62311_62312delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+18156_502+18157delinsAT MANE Select	ENSP00000279873.7:n.502+18156_502+18157delinsAT
ENST00000644638.1:c.502+18156_502+18157delinsAT	ENSP00000494412.1:n.502+18156_502+18157delinsAT
ENST00000681100.1:c.502+18156_502+18157delinsAT	ENSP00000506119.1:n.502+18156_502+18157delinsAT
ENST00000279873.11:c.502+18156_502+18157delinsAT	ENSP00000279873.7:n.502+18156_502+18157delinsAT
NM_032199.2:c.502+18156_502+18157delinsAT	NP_115575.1:n.502+18156_502+18157delinsAT
XM_011540262.1:c.502+18156_502+18157delinsAT	XP_011538564.1:n.502+18156_502+18157delinsAT
XM_024448230.1:c.-66+18156_-66+18157delinsAT	XP_024303998.1:n.-66+18156_-66+18157delinsAT
NM_032199.3:c.502+18156_502+18157delinsAT MANE Select	NP_115575.1:n.502+18156_502+18157delinsAT