Canonical Allele Identifier: CA14051862

Gene: FOXN3

Linked Data

• dbSNP Id: rs8004664
• gnomAD v2: 14-90034972-G-A
• gnomAD v3: 14-89568628-G-A
• gnomAD v4: 14-89568628-G-A
• MyVariant Identifiers: chr14:g.90034972G>A (hg19) ; chr14:g.89568628G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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