Canonical Allele Identifier: CA965801573
Gene: FOXN3 HGNC NCBI

Linked Data

dbSNP Id: rs1895418147

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.89568650T>G , CM000676.2:g.89568650T>G GRCh38
NC_000014.8:g.90034994T>G , CM000676.1:g.90034994T>G GRCh37
NC_000014.7:g.89104747T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000345097.8:c.-15+50378A>C ENSP00000343288.4:n.-15+50378A>C
ENST00000555353.5:c.-15+50378A>C ENSP00000452227.1:n.-15+50378A>C
ENST00000555855.5:c.-118+50378A>C ENSP00000451135.1:n.-118+50378A>C
NM_001085471.1:c.-15+50378A>C NP_001078940.1:n.-15+50378A>C
NM_001085471.2:c.-15+50378A>C NP_001078940.1:n.-15+50378A>C