Canonical Allele Identifier: CA2690187545
Gene: FXN HGNC NCBI

Linked Data

gnomAD v4: 9-69035685-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035685C>A , CM000671.2:g.69035685C>A GRCh38
NC_000009.11:g.71650601C>A , CM000671.1:g.71650601C>A GRCh37
NC_000009.10:g.70840421C>A NCBI36
NG_008845.2:g.5123C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-98C>A ENSP00000366482.3:n.-98C>A
ENST00000396364.7:c.-98C>A ENSP00000379650.3:n.-98C>A
NM_000144.4:c.-98C>A NP_000135.2:n.-98C>A
NM_001161706.1:c.-98C>A NP_001155178.1:n.-98C>A
NM_181425.2:c.-98C>A NP_852090.1:n.-98C>A