Canonical Allele Identifier: CA1914339045
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992191_61992192delinsTC , CM000672.2:g.61992191_61992192delinsTC GRCh38
NC_000010.10:g.63751950_63751951delinsTC , CM000672.1:g.63751950_63751951delinsTC GRCh37
NC_000010.9:g.63421956_63421957delinsTC NCBI36
NG_030027.1:g.95938_95939delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-7900_503-7899delinsTC MANE Select ENSP00000279873.7:n.503-7900_503-7899delinsTC
ENST00000644638.1:c.503-7900_503-7899delinsTC ENSP00000494412.1:n.503-7900_503-7899delinsTC
ENST00000681100.1:c.503-7900_503-7899delinsTC ENSP00000506119.1:n.503-7900_503-7899delinsTC
ENST00000279873.11:c.503-7900_503-7899delinsTC ENSP00000279873.7:n.503-7900_503-7899delinsTC
NM_032199.2:c.503-7900_503-7899delinsTC NP_115575.1:n.503-7900_503-7899delinsTC
XM_011540262.1:c.502+51783_502+51784delinsTC XP_011538564.1:n.502+51783_502+51784delinsTC
XM_024448230.1:c.-65-7900_-65-7899delinsTC XP_024303998.1:n.-65-7900_-65-7899delinsTC
NM_032199.3:c.503-7900_503-7899delinsTC MANE Select NP_115575.1:n.503-7900_503-7899delinsTC