Canonical Allele Identifier: CA1914338116

Gene: ARID5B

Linked Data

• dbSNP Id: rs1838866808

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61987739del , CM000672.2:g.61987739del	GRCh38
NC_000010.10:g.63747498del , CM000672.1:g.63747498del	GRCh37
NC_000010.9:g.63417504del	NCBI36
NG_030027.1:g.91486del

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.503-12352del MANE Select	ENSP00000279873.7:n.503-12352del
ENST00000644638.1:c.503-12352del	ENSP00000494412.1:n.503-12352del
ENST00000681100.1:c.503-12352del	ENSP00000506119.1:n.503-12352del
ENST00000279873.11:c.503-12352del	ENSP00000279873.7:n.503-12352del
NM_032199.2:c.503-12352del	NP_115575.1:n.503-12352del
XM_011540262.1:c.502+47331del	XP_011538564.1:n.502+47331del
XM_024448230.1:c.-65-12352del	XP_024303998.1:n.-65-12352del
NM_032199.3:c.503-12352del MANE Select	NP_115575.1:n.503-12352del