Canonical Allele Identifier: CA208540789

Gene: ARID5B

Linked Data

• dbSNP Id: rs924496683
• gnomAD v3: 10-61935153-T-G
• gnomAD v4: 10-61935153-T-G
• MyVariant Identifiers: chr10:g.63694912T>G (hg19) ; chr10:g.61935153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61935153T>G , CM000672.2:g.61935153T>G	GRCh38
NC_000010.10:g.63694912T>G , CM000672.1:g.63694912T>G	GRCh37
NC_000010.9:g.63364918T>G	NCBI36
NG_030027.1:g.38900T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.277-5030T>G MANE Select	ENSP00000279873.7:n.277-5030T>G
ENST00000644638.1:c.277-5030T>G	ENSP00000494412.1:n.277-5030T>G
ENST00000681100.1:c.277-5030T>G	ENSP00000506119.1:n.277-5030T>G
ENST00000279873.11:c.277-5030T>G	ENSP00000279873.7:n.277-5030T>G
NM_032199.2:c.277-5030T>G	NP_115575.1:n.277-5030T>G
XM_011540262.1:c.277-5030T>G	XP_011538564.1:n.277-5030T>G
XM_024448230.1:c.-291-5030T>G	XP_024303998.1:n.-291-5030T>G
NM_032199.3:c.277-5030T>G MANE Select	NP_115575.1:n.277-5030T>G