Canonical Allele Identifier: CA1914351999
Gene: ARID5B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62019943G= , CM000672.2:g.62019943G= GRCh38
NC_000010.10:g.63779702G= , CM000672.1:g.63779702G= GRCh37
NC_000010.9:g.63449708G= NCBI36
NG_030027.1:g.123690G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.733+19622G= MANE Select ENSP00000279873.7:n.733+19622G=
ENST00000644638.1:c.734-4730G= ENSP00000494412.1:n.734-4730G=
ENST00000681100.1:c.733+19622G= ENSP00000506119.1:n.733+19622G=
ENST00000279873.11:c.733+19622G= ENSP00000279873.7:n.733+19622G=
NM_032199.2:c.733+19622G= NP_115575.1:n.733+19622G=
XM_011540262.1:c.503-30945G= XP_011538564.1:n.503-30945G=
XM_024448230.1:c.166+19622G= XP_024303998.1:n.166+19622G=
NM_032199.3:c.733+19622G= MANE Select NP_115575.1:n.733+19622G=
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