Canonical Allele Identifier: CA208335953

Gene: ARID5B

Linked Data

• dbSNP Id: rs915967311
• gnomAD v3: 10-62019949-C-G
• gnomAD v4: 10-62019949-C-G
• MyVariant Identifiers: chr10:g.63779708C>G (hg19) ; chr10:g.62019949C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62019949C>G , CM000672.2:g.62019949C>G	GRCh38
NC_000010.10:g.63779708C>G , CM000672.1:g.63779708C>G	GRCh37
NC_000010.9:g.63449714C>G	NCBI36
NG_030027.1:g.123696C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.733+19628C>G MANE Select	ENSP00000279873.7:n.733+19628C>G
ENST00000644638.1:c.734-4724C>G	ENSP00000494412.1:n.734-4724C>G
ENST00000681100.1:c.733+19628C>G	ENSP00000506119.1:n.733+19628C>G
ENST00000279873.11:c.733+19628C>G	ENSP00000279873.7:n.733+19628C>G
NM_032199.2:c.733+19628C>G	NP_115575.1:n.733+19628C>G
XM_011540262.1:c.503-30939C>G	XP_011538564.1:n.503-30939C>G
XM_024448230.1:c.166+19628C>G	XP_024303998.1:n.166+19628C>G
NM_032199.3:c.733+19628C>G MANE Select	NP_115575.1:n.733+19628C>G