Canonical Allele Identifier: CA1914337263
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838839053

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61985807_61985809del , CM000672.2:g.61985807_61985809del GRCh38
NC_000010.10:g.63745566_63745568del , CM000672.1:g.63745566_63745568del GRCh37
NC_000010.9:g.63415572_63415574del NCBI36
NG_030027.1:g.89554_89556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-14284_503-14282del MANE Select ENSP00000279873.7:n.503-14284_503-14282del
ENST00000644638.1:c.503-14284_503-14282del ENSP00000494412.1:n.503-14284_503-14282del
ENST00000681100.1:c.503-14284_503-14282del ENSP00000506119.1:n.503-14284_503-14282del
ENST00000279873.11:c.503-14284_503-14282del ENSP00000279873.7:n.503-14284_503-14282del
NM_032199.2:c.503-14284_503-14282del NP_115575.1:n.503-14284_503-14282del
XM_011540262.1:c.502+45399_502+45401del XP_011538564.1:n.502+45399_502+45401del
XM_024448230.1:c.-65-14284_-65-14282del XP_024303998.1:n.-65-14284_-65-14282del
NM_032199.3:c.503-14284_503-14282del MANE Select NP_115575.1:n.503-14284_503-14282del