Canonical Allele Identifier: CA667198983

Gene: ARID5B

Linked Data

• dbSNP Id: rs1336549512
• gnomAD v3: 10-61935217-C-G
• gnomAD v4: 10-61935217-C-G
• MyVariant Identifiers: chr10:g.63694976C>G (hg19) ; chr10:g.61935217C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61935217C>G , CM000672.2:g.61935217C>G	GRCh38
NC_000010.10:g.63694976C>G , CM000672.1:g.63694976C>G	GRCh37
NC_000010.9:g.63364982C>G	NCBI36
NG_030027.1:g.38964C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.277-4966C>G MANE Select	ENSP00000279873.7:n.277-4966C>G
ENST00000644638.1:c.277-4966C>G	ENSP00000494412.1:n.277-4966C>G
ENST00000681100.1:c.277-4966C>G	ENSP00000506119.1:n.277-4966C>G
ENST00000279873.11:c.277-4966C>G	ENSP00000279873.7:n.277-4966C>G
NM_032199.2:c.277-4966C>G	NP_115575.1:n.277-4966C>G
XM_011540262.1:c.277-4966C>G	XP_011538564.1:n.277-4966C>G
XM_024448230.1:c.-291-4966C>G	XP_024303998.1:n.-291-4966C>G
NM_032199.3:c.277-4966C>G MANE Select	NP_115575.1:n.277-4966C>G