Canonical Allele Identifier: CA1914352008
Gene: ARID5B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62019966T= , CM000672.2:g.62019966T= GRCh38
NC_000010.10:g.63779725T= , CM000672.1:g.63779725T= GRCh37
NC_000010.9:g.63449731T= NCBI36
NG_030027.1:g.123713T=

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.733+19645T= MANE Select ENSP00000279873.7:n.733+19645T=
ENST00000644638.1:c.734-4707T= ENSP00000494412.1:n.734-4707T=
ENST00000681100.1:c.733+19645T= ENSP00000506119.1:n.733+19645T=
ENST00000279873.11:c.733+19645T= ENSP00000279873.7:n.733+19645T=
NM_032199.2:c.733+19645T= NP_115575.1:n.733+19645T=
XM_011540262.1:c.503-30922T= XP_011538564.1:n.503-30922T=
XM_024448230.1:c.166+19645T= XP_024303998.1:n.166+19645T=
NM_032199.3:c.733+19645T= MANE Select NP_115575.1:n.733+19645T=
Search 100 bp 5'
Search 100 bp 3'