Canonical Allele Identifier: CA929076350
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838934230

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992116dup , CM000672.2:g.61992116dup GRCh38
NC_000010.10:g.63751875dup , CM000672.1:g.63751875dup GRCh37
NC_000010.9:g.63421881dup NCBI36
NG_030027.1:g.95863dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-7975dup MANE Select ENSP00000279873.7:n.503-7975dup
ENST00000644638.1:c.503-7975dup ENSP00000494412.1:n.503-7975dup
ENST00000681100.1:c.503-7975dup ENSP00000506119.1:n.503-7975dup
ENST00000279873.11:c.503-7975dup ENSP00000279873.7:n.503-7975dup
NM_032199.2:c.503-7975dup NP_115575.1:n.503-7975dup
XM_011540262.1:c.502+51708dup XP_011538564.1:n.502+51708dup
XM_024448230.1:c.-65-7975dup XP_024303998.1:n.-65-7975dup
NM_032199.3:c.503-7975dup MANE Select NP_115575.1:n.503-7975dup