Canonical Allele Identifier: CA667222815

Gene: ARID5B

Linked Data

• dbSNP Id: rs1381513305
• MyVariant Identifiers: chr10:g.63747706A>G (hg19) ; chr10:g.61987947A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61987947A>G , CM000672.2:g.61987947A>G	GRCh38
NC_000010.10:g.63747706A>G , CM000672.1:g.63747706A>G	GRCh37
NC_000010.9:g.63417712A>G	NCBI36
NG_030027.1:g.91694A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.503-12144A>G MANE Select	ENSP00000279873.7:n.503-12144A>G
ENST00000644638.1:c.503-12144A>G	ENSP00000494412.1:n.503-12144A>G
ENST00000681100.1:c.503-12144A>G	ENSP00000506119.1:n.503-12144A>G
ENST00000279873.11:c.503-12144A>G	ENSP00000279873.7:n.503-12144A>G
NM_032199.2:c.503-12144A>G	NP_115575.1:n.503-12144A>G
XM_011540262.1:c.502+47539A>G	XP_011538564.1:n.502+47539A>G
XM_024448230.1:c.-65-12144A>G	XP_024303998.1:n.-65-12144A>G
NM_032199.3:c.503-12144A>G MANE Select	NP_115575.1:n.503-12144A>G