Canonical Allele Identifier: CA2579347217
Gene: FXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035713C>G , CM000671.2:g.69035713C>G GRCh38
NC_000009.11:g.71650629C>G , CM000671.1:g.71650629C>G GRCh37
NC_000009.10:g.70840449C>G NCBI36
NG_008845.2:g.5151C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377270.7:c.-70C>G ENSP00000366482.3:n.-70C>G
ENST00000396364.7:c.-70C>G ENSP00000379650.3:n.-70C>G
NM_000144.4:c.-70C>G NP_000135.2:n.-70C>G
NM_001161706.1:c.-70C>G NP_001155178.1:n.-70C>G
NM_181425.2:c.-70C>G NP_852090.1:n.-70C>G