Canonical Allele Identifier: CA709735661
Gene: FOXN3 HGNC NCBI

Linked Data

dbSNP Id: rs8004664
MyVariant Identifiers: chr14:g.90034972G>C (hg19) chr14:g.89568628G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.89568628G>C , CM000676.2:g.89568628G>C GRCh38
NC_000014.8:g.90034972G>C , CM000676.1:g.90034972G>C GRCh37
NC_000014.7:g.89104725G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000345097.8:c.-15+50400C>G ENSP00000343288.4:n.-15+50400C>G
ENST00000555353.5:c.-15+50400C>G ENSP00000452227.1:n.-15+50400C>G
ENST00000555855.5:c.-118+50400C>G ENSP00000451135.1:n.-118+50400C>G
NM_001085471.1:c.-15+50400C>G NP_001078940.1:n.-15+50400C>G
NM_001085471.2:c.-15+50400C>G NP_001078940.1:n.-15+50400C>G
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