Canonical Allele Identifier: CA1854034847
Gene: FXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035686T= , CM000671.2:g.69035686T= GRCh38
NC_000009.11:g.71650602T= , CM000671.1:g.71650602T= GRCh37
NC_000009.10:g.70840422T= NCBI36
NG_008845.2:g.5124T=

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-97T= ENSP00000366482.3:n.-97T=
ENST00000396364.7:c.-97T= ENSP00000379650.3:n.-97T=
NM_000144.4:c.-97T= NP_000135.2:n.-97T=
NM_001161706.1:c.-97T= NP_001155178.1:n.-97T=
NM_181425.2:c.-97T= NP_852090.1:n.-97T=