Canonical Allele Identifier: CA667212097

Gene: ARID5B

Linked Data

• dbSNP Id: rs1292174117
• gnomAD v3: 10-62020174-TG-T
• gnomAD v4: 10-62020174-TG-T
• MyVariant Identifiers: chr10:g.63779934del (hg19) ; chr10:g.62020175del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62020177del , CM000672.2:g.62020177del	GRCh38
NC_000010.10:g.63779936del , CM000672.1:g.63779936del	GRCh37
NC_000010.9:g.63449942del	NCBI36
NG_030027.1:g.123924del

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.733+19856del MANE Select	ENSP00000279873.7:n.733+19856del
ENST00000644638.1:c.734-4496del	ENSP00000494412.1:n.734-4496del
ENST00000681100.1:c.733+19856del	ENSP00000506119.1:n.733+19856del
ENST00000279873.11:c.733+19856del	ENSP00000279873.7:n.733+19856del
NM_032199.2:c.733+19856del	NP_115575.1:n.733+19856del
XM_011540262.1:c.503-30711del	XP_011538564.1:n.503-30711del
XM_024448230.1:c.166+19856del	XP_024303998.1:n.166+19856del
NM_032199.3:c.733+19856del MANE Select	NP_115575.1:n.733+19856del