Canonical Allele Identifier: CA615927215
Gene: FOXN3 HGNC NCBI

Linked Data

dbSNP Id: rs1391809923
gnomAD v2: 14-90035070-C-A
gnomAD v3: 14-89568726-C-A
gnomAD v4: 14-89568726-C-A
MyVariant Identifiers: chr14:g.90035070C>A (hg19) chr14:g.89568726C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.89568726C>A , CM000676.2:g.89568726C>A GRCh38
NC_000014.8:g.90035070C>A , CM000676.1:g.90035070C>A GRCh37
NC_000014.7:g.89104823C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000345097.8:c.-15+50302G>T ENSP00000343288.4:n.-15+50302G>T
ENST00000555353.5:c.-15+50302G>T ENSP00000452227.1:n.-15+50302G>T
ENST00000555855.5:c.-118+50302G>T ENSP00000451135.1:n.-118+50302G>T
NM_001085471.1:c.-15+50302G>T NP_001078940.1:n.-15+50302G>T
NM_001085471.2:c.-15+50302G>T NP_001078940.1:n.-15+50302G>T
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