Canonical Allele Identifier: CA594019388

Gene: ARID5B

Linked Data

• dbSNP Id: rs1373724248
• gnomAD v2: 10-63721123-T-G
• gnomAD v3: 10-61961364-T-G
• gnomAD v4: 10-61961364-T-G
• MyVariant Identifiers: chr10:g.63721123T>G (hg19) ; chr10:g.61961364T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61961364T>G , CM000672.2:g.61961364T>G	GRCh38
NC_000010.10:g.63721123T>G , CM000672.1:g.63721123T>G	GRCh37
NC_000010.9:g.63391129T>G	NCBI36
NG_030027.1:g.65111T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.502+20956T>G MANE Select	ENSP00000279873.7:n.502+20956T>G
ENST00000644638.1:c.502+20956T>G	ENSP00000494412.1:n.502+20956T>G
ENST00000681100.1:c.502+20956T>G	ENSP00000506119.1:n.502+20956T>G
ENST00000279873.11:c.502+20956T>G	ENSP00000279873.7:n.502+20956T>G
NM_032199.2:c.502+20956T>G	NP_115575.1:n.502+20956T>G
XM_011540262.1:c.502+20956T>G	XP_011538564.1:n.502+20956T>G
XM_024448230.1:c.-66+20956T>G	XP_024303998.1:n.-66+20956T>G
NM_032199.3:c.502+20956T>G MANE Select	NP_115575.1:n.502+20956T>G