Canonical Allele Identifier: CA1914352020
Gene: ARID5B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62019990C= , CM000672.2:g.62019990C= GRCh38
NC_000010.10:g.63779749C= , CM000672.1:g.63779749C= GRCh37
NC_000010.9:g.63449755C= NCBI36
NG_030027.1:g.123737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.733+19669C= MANE Select ENSP00000279873.7:n.733+19669C=
ENST00000644638.1:c.734-4683C= ENSP00000494412.1:n.734-4683C=
ENST00000681100.1:c.733+19669C= ENSP00000506119.1:n.733+19669C=
ENST00000279873.11:c.733+19669C= ENSP00000279873.7:n.733+19669C=
NM_032199.2:c.733+19669C= NP_115575.1:n.733+19669C=
XM_011540262.1:c.503-30898C= XP_011538564.1:n.503-30898C=
XM_024448230.1:c.166+19669C= XP_024303998.1:n.166+19669C=
NM_032199.3:c.733+19669C= MANE Select NP_115575.1:n.733+19669C=
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