Canonical Allele Identifier: CA1914338124
Gene: ARID5B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61987766C= , CM000672.2:g.61987766C= GRCh38
NC_000010.10:g.63747525C= , CM000672.1:g.63747525C= GRCh37
NC_000010.9:g.63417531C= NCBI36
NG_030027.1:g.91513C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.503-12325C= MANE Select ENSP00000279873.7:n.503-12325C=
ENST00000644638.1:c.503-12325C= ENSP00000494412.1:n.503-12325C=
ENST00000681100.1:c.503-12325C= ENSP00000506119.1:n.503-12325C=
ENST00000279873.11:c.503-12325C= ENSP00000279873.7:n.503-12325C=
NM_032199.2:c.503-12325C= NP_115575.1:n.503-12325C=
XM_011540262.1:c.502+47358C= XP_011538564.1:n.502+47358C=
XM_024448230.1:c.-65-12325C= XP_024303998.1:n.-65-12325C=
NM_032199.3:c.503-12325C= MANE Select NP_115575.1:n.503-12325C=
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