Canonical Allele Identifier: CA667198927

Gene: ARID5B

Linked Data

• dbSNP Id: rs1282266367
• MyVariant Identifiers: chr10:g.63694853A>C (hg19) ; chr10:g.61935094A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61935094A>C , CM000672.2:g.61935094A>C	GRCh38
NC_000010.10:g.63694853A>C , CM000672.1:g.63694853A>C	GRCh37
NC_000010.9:g.63364859A>C	NCBI36
NG_030027.1:g.38841A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.277-5089A>C MANE Select	ENSP00000279873.7:n.277-5089A>C
ENST00000644638.1:c.277-5089A>C	ENSP00000494412.1:n.277-5089A>C
ENST00000681100.1:c.277-5089A>C	ENSP00000506119.1:n.277-5089A>C
ENST00000279873.11:c.277-5089A>C	ENSP00000279873.7:n.277-5089A>C
NM_032199.2:c.277-5089A>C	NP_115575.1:n.277-5089A>C
XM_011540262.1:c.277-5089A>C	XP_011538564.1:n.277-5089A>C
XM_024448230.1:c.-291-5089A>C	XP_024303998.1:n.-291-5089A>C
NM_032199.3:c.277-5089A>C MANE Select	NP_115575.1:n.277-5089A>C