Canonical Allele Identifier: CA1854034850
Gene: FXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035690C= , CM000671.2:g.69035690C= GRCh38
NC_000009.11:g.71650606C= , CM000671.1:g.71650606C= GRCh37
NC_000009.10:g.70840426C= NCBI36
NG_008845.2:g.5128C=

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-93C= ENSP00000366482.3:n.-93C=
ENST00000396364.7:c.-93C= ENSP00000379650.3:n.-93C=
NM_000144.4:c.-93C= NP_000135.2:n.-93C=
NM_001161706.1:c.-93C= NP_001155178.1:n.-93C=
NM_181425.2:c.-93C= NP_852090.1:n.-93C=