Canonical Allele Identifier: CA208543991

Gene: ARID5B

Linked Data

• dbSNP Id: rs763042650
• gnomAD v2: 10-63723406-GC-G
• gnomAD v3: 10-61963647-GC-G
• gnomAD v4: 10-61963647-GC-G
• MyVariant Identifiers: chr10:g.63723407del (hg19) ; chr10:g.61963648del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61963651del , CM000672.2:g.61963651del	GRCh38
NC_000010.10:g.63723410del , CM000672.1:g.63723410del	GRCh37
NC_000010.9:g.63393416del	NCBI36
NG_030027.1:g.67398del

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+23243del MANE Select	ENSP00000279873.7:n.502+23243del
ENST00000644638.1:c.502+23243del	ENSP00000494412.1:n.502+23243del
ENST00000681100.1:c.502+23243del	ENSP00000506119.1:n.502+23243del
ENST00000279873.11:c.502+23243del	ENSP00000279873.7:n.502+23243del
NM_032199.2:c.502+23243del	NP_115575.1:n.502+23243del
XM_011540262.1:c.502+23243del	XP_011538564.1:n.502+23243del
XM_024448230.1:c.-66+23243del	XP_024303998.1:n.-66+23243del
NM_032199.3:c.502+23243del MANE Select	NP_115575.1:n.502+23243del