Canonical Allele Identifier: CA2690187587
Gene: FXN HGNC NCBI

Linked Data

gnomAD v4: 9-69035717-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035717T>G , CM000671.2:g.69035717T>G GRCh38
NC_000009.11:g.71650633T>G , CM000671.1:g.71650633T>G GRCh37
NC_000009.10:g.70840453T>G NCBI36
NG_008845.2:g.5155T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-66T>G ENSP00000366482.3:n.-66T>G
ENST00000396364.7:c.-66T>G ENSP00000379650.3:n.-66T>G
NM_000144.4:c.-66T>G NP_000135.2:n.-66T>G
NM_001161706.1:c.-66T>G NP_001155178.1:n.-66T>G
NM_181425.2:c.-66T>G NP_852090.1:n.-66T>G
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