Canonical Allele Identifier: CA929066156

Gene: ARID5B

Linked Data

• dbSNP Id: rs1838507427
• gnomAD v3: 10-61963833-G-GCAC
• gnomAD v4: 10-61963833-G-GCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963835_61963837dup , CM000672.2:g.61963835_61963837dup	GRCh38
NC_000010.10:g.63723594_63723596dup , CM000672.1:g.63723594_63723596dup	GRCh37
NC_000010.9:g.63393600_63393602dup	NCBI36
NG_030027.1:g.67582_67584dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+23427_502+23429dup MANE Select	ENSP00000279873.7:n.502+23427_502+23429dup
ENST00000644638.1:c.502+23427_502+23429dup	ENSP00000494412.1:n.502+23427_502+23429dup
ENST00000681100.1:c.502+23427_502+23429dup	ENSP00000506119.1:n.502+23427_502+23429dup
ENST00000279873.11:c.502+23427_502+23429dup	ENSP00000279873.7:n.502+23427_502+23429dup
NM_032199.2:c.502+23427_502+23429dup	NP_115575.1:n.502+23427_502+23429dup
XM_011540262.1:c.502+23427_502+23429dup	XP_011538564.1:n.502+23427_502+23429dup
XM_024448230.1:c.-66+23427_-66+23429dup	XP_024303998.1:n.-66+23427_-66+23429dup
NM_032199.3:c.502+23427_502+23429dup MANE Select	NP_115575.1:n.502+23427_502+23429dup