Canonical Allele Identifier: CA667209068

Gene: ARID5B

Linked Data

• dbSNP Id: rs1159348914
• gnomAD v3: 10-61958447-A-G
• gnomAD v4: 10-61958447-A-G
• MyVariant Identifiers: chr10:g.63718206A>G (hg19) ; chr10:g.61958447A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61958447A>G , CM000672.2:g.61958447A>G	GRCh38
NC_000010.10:g.63718206A>G , CM000672.1:g.63718206A>G	GRCh37
NC_000010.9:g.63388212A>G	NCBI36
NG_030027.1:g.62194A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.502+18039A>G MANE Select	ENSP00000279873.7:n.502+18039A>G
ENST00000644638.1:c.502+18039A>G	ENSP00000494412.1:n.502+18039A>G
ENST00000681100.1:c.502+18039A>G	ENSP00000506119.1:n.502+18039A>G
ENST00000279873.11:c.502+18039A>G	ENSP00000279873.7:n.502+18039A>G
NM_032199.2:c.502+18039A>G	NP_115575.1:n.502+18039A>G
XM_011540262.1:c.502+18039A>G	XP_011538564.1:n.502+18039A>G
XM_024448230.1:c.-66+18039A>G	XP_024303998.1:n.-66+18039A>G
NM_032199.3:c.502+18039A>G MANE Select	NP_115575.1:n.502+18039A>G