Canonical Allele Identifier: CA1914339118
Gene: ARID5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61992295_61992297delinsGAA , CM000672.2:g.61992295_61992297delinsGAA GRCh38
NC_000010.10:g.63752054_63752056delinsGAA , CM000672.1:g.63752054_63752056delinsGAA GRCh37
NC_000010.9:g.63422060_63422062delinsGAA NCBI36
NG_030027.1:g.96042_96044delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-7796_503-7794delinsGAA MANE Select ENSP00000279873.7:n.503-7796_503-7794delinsGAA
ENST00000644638.1:c.503-7796_503-7794delinsGAA ENSP00000494412.1:n.503-7796_503-7794delinsGAA
ENST00000681100.1:c.503-7796_503-7794delinsGAA ENSP00000506119.1:n.503-7796_503-7794delinsGAA
ENST00000279873.11:c.503-7796_503-7794delinsGAA ENSP00000279873.7:n.503-7796_503-7794delinsGAA
NM_032199.2:c.503-7796_503-7794delinsGAA NP_115575.1:n.503-7796_503-7794delinsGAA
XM_011540262.1:c.502+51887_502+51889delinsGAA XP_011538564.1:n.502+51887_502+51889delinsGAA
XM_024448230.1:c.-65-7796_-65-7794delinsGAA XP_024303998.1:n.-65-7796_-65-7794delinsGAA
NM_032199.3:c.503-7796_503-7794delinsGAA MANE Select NP_115575.1:n.503-7796_503-7794delinsGAA