Canonical Allele Identifier: CA1914352058
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1839336662

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62020102dup , CM000672.2:g.62020102dup GRCh38
NC_000010.10:g.63779861dup , CM000672.1:g.63779861dup GRCh37
NC_000010.9:g.63449867dup NCBI36
NG_030027.1:g.123849dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.733+19781dup MANE Select ENSP00000279873.7:n.733+19781dup
ENST00000644638.1:c.734-4571dup ENSP00000494412.1:n.734-4571dup
ENST00000681100.1:c.733+19781dup ENSP00000506119.1:n.733+19781dup
ENST00000279873.11:c.733+19781dup ENSP00000279873.7:n.733+19781dup
NM_032199.2:c.733+19781dup NP_115575.1:n.733+19781dup
XM_011540262.1:c.503-30786dup XP_011538564.1:n.503-30786dup
XM_024448230.1:c.166+19781dup XP_024303998.1:n.166+19781dup
NM_032199.3:c.733+19781dup MANE Select NP_115575.1:n.733+19781dup