Canonical Allele Identifier: CA667212087

Gene: ARID5B

Linked Data

• dbSNP Id: rs1355809199
• gnomAD v3: 10-62020119-G-A
• gnomAD v4: 10-62020119-G-A
• MyVariant Identifiers: chr10:g.63779878G>A (hg19) ; chr10:g.62020119G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62020119G>A , CM000672.2:g.62020119G>A	GRCh38
NC_000010.10:g.63779878G>A , CM000672.1:g.63779878G>A	GRCh37
NC_000010.9:g.63449884G>A	NCBI36
NG_030027.1:g.123866G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.733+19798G>A MANE Select	ENSP00000279873.7:n.733+19798G>A
ENST00000644638.1:c.734-4554G>A	ENSP00000494412.1:n.734-4554G>A
ENST00000681100.1:c.733+19798G>A	ENSP00000506119.1:n.733+19798G>A
ENST00000279873.11:c.733+19798G>A	ENSP00000279873.7:n.733+19798G>A
NM_032199.2:c.733+19798G>A	NP_115575.1:n.733+19798G>A
XM_011540262.1:c.503-30769G>A	XP_011538564.1:n.503-30769G>A
XM_024448230.1:c.166+19798G>A	XP_024303998.1:n.166+19798G>A
NM_032199.3:c.733+19798G>A MANE Select	NP_115575.1:n.733+19798G>A