Canonical Allele Identifier: CA929076895
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1844277070

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61935133dup , CM000672.2:g.61935133dup GRCh38
NC_000010.10:g.63694892dup , CM000672.1:g.63694892dup GRCh37
NC_000010.9:g.63364898dup NCBI36
NG_030027.1:g.38880dup

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.277-5050dup MANE Select ENSP00000279873.7:n.277-5050dup
ENST00000644638.1:c.277-5050dup ENSP00000494412.1:n.277-5050dup
ENST00000681100.1:c.277-5050dup ENSP00000506119.1:n.277-5050dup
ENST00000279873.11:c.277-5050dup ENSP00000279873.7:n.277-5050dup
NM_032199.2:c.277-5050dup NP_115575.1:n.277-5050dup
XM_011540262.1:c.277-5050dup XP_011538564.1:n.277-5050dup
XM_024448230.1:c.-291-5050dup XP_024303998.1:n.-291-5050dup
NM_032199.3:c.277-5050dup MANE Select NP_115575.1:n.277-5050dup