Canonical Allele Identifier: CA918689204

Gene: ARID5B

Linked Data

• dbSNP Id: rs1589237325
• gnomAD v3: 10-61963631-CTTT-C
• gnomAD v4: 10-61963631-CTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963632_61963634del , CM000672.2:g.61963632_61963634del	GRCh38
NC_000010.10:g.63723391_63723393del , CM000672.1:g.63723391_63723393del	GRCh37
NC_000010.9:g.63393397_63393399del	NCBI36
NG_030027.1:g.67379_67381del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+23224_502+23226del MANE Select	ENSP00000279873.7:n.502+23224_502+23226del
ENST00000644638.1:c.502+23224_502+23226del	ENSP00000494412.1:n.502+23224_502+23226del
ENST00000681100.1:c.502+23224_502+23226del	ENSP00000506119.1:n.502+23224_502+23226del
ENST00000279873.11:c.502+23224_502+23226del	ENSP00000279873.7:n.502+23224_502+23226del
NM_032199.2:c.502+23224_502+23226del	NP_115575.1:n.502+23224_502+23226del
XM_011540262.1:c.502+23224_502+23226del	XP_011538564.1:n.502+23224_502+23226del
XM_024448230.1:c.-66+23224_-66+23226del	XP_024303998.1:n.-66+23224_-66+23226del
NM_032199.3:c.502+23224_502+23226del MANE Select	NP_115575.1:n.502+23224_502+23226del