Canonical Allele Identifier: CA1914338163
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61987866_61987867delinsAT , CM000672.2:g.61987866_61987867delinsAT GRCh38
NC_000010.10:g.63747625_63747626delinsAT , CM000672.1:g.63747625_63747626delinsAT GRCh37
NC_000010.9:g.63417631_63417632delinsAT NCBI36
NG_030027.1:g.91613_91614delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-12225_503-12224delinsAT MANE Select ENSP00000279873.7:n.503-12225_503-12224delinsAT
ENST00000644638.1:c.503-12225_503-12224delinsAT ENSP00000494412.1:n.503-12225_503-12224delinsAT
ENST00000681100.1:c.503-12225_503-12224delinsAT ENSP00000506119.1:n.503-12225_503-12224delinsAT
ENST00000279873.11:c.503-12225_503-12224delinsAT ENSP00000279873.7:n.503-12225_503-12224delinsAT
NM_032199.2:c.503-12225_503-12224delinsAT NP_115575.1:n.503-12225_503-12224delinsAT
XM_011540262.1:c.502+47458_502+47459delinsAT XP_011538564.1:n.502+47458_502+47459delinsAT
XM_024448230.1:c.-65-12225_-65-12224delinsAT XP_024303998.1:n.-65-12225_-65-12224delinsAT
NM_032199.3:c.503-12225_503-12224delinsAT MANE Select NP_115575.1:n.503-12225_503-12224delinsAT