Canonical Allele Identifier: CA1854034812
Gene: FXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035598G= , CM000671.2:g.69035598G= GRCh38
NC_000009.11:g.71650514G= , CM000671.1:g.71650514G= GRCh37
NC_000009.10:g.70840334G= NCBI36
NG_008845.2:g.5036G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377270.7:c.-185G= ENSP00000366482.3:n.-185G=
ENST00000396364.7:c.-185G= ENSP00000379650.3:n.-185G=
NM_000144.4:c.-185G= NP_000135.2:n.-185G=
NM_001161706.1:c.-185G= NP_001155178.1:n.-185G=
NM_181425.2:c.-185G= NP_852090.1:n.-185G=