Canonical Allele Identifier: CA593888735

Gene: ARID5B

Linked Data

• dbSNP Id: rs1359914382
• gnomAD v2: 10-63779762-A-G
• MyVariant Identifiers: chr10:g.63779762A>G (hg19) ; chr10:g.62020003A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62020003A>G , CM000672.2:g.62020003A>G	GRCh38
NC_000010.10:g.63779762A>G , CM000672.1:g.63779762A>G	GRCh37
NC_000010.9:g.63449768A>G	NCBI36
NG_030027.1:g.123750A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.733+19682A>G MANE Select	ENSP00000279873.7:n.733+19682A>G
ENST00000644638.1:c.734-4670A>G	ENSP00000494412.1:n.734-4670A>G
ENST00000681100.1:c.733+19682A>G	ENSP00000506119.1:n.733+19682A>G
ENST00000279873.11:c.733+19682A>G	ENSP00000279873.7:n.733+19682A>G
NM_032199.2:c.733+19682A>G	NP_115575.1:n.733+19682A>G
XM_011540262.1:c.503-30885A>G	XP_011538564.1:n.503-30885A>G
XM_024448230.1:c.166+19682A>G	XP_024303998.1:n.166+19682A>G
NM_032199.3:c.733+19682A>G MANE Select	NP_115575.1:n.733+19682A>G