Canonical Allele Identifier: CA2154077293
Gene: FOXN3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.89568695T= , CM000676.2:g.89568695T= GRCh38
NC_000014.8:g.90035039T= , CM000676.1:g.90035039T= GRCh37
NC_000014.7:g.89104792T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000345097.8:c.-15+50333A= ENSP00000343288.4:n.-15+50333A=
ENST00000555353.5:c.-15+50333A= ENSP00000452227.1:n.-15+50333A=
ENST00000555855.5:c.-118+50333A= ENSP00000451135.1:n.-118+50333A=
NM_001085471.1:c.-15+50333A= NP_001078940.1:n.-15+50333A=
NM_001085471.2:c.-15+50333A= NP_001078940.1:n.-15+50333A=
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