Canonical Allele Identifier: CA2690187571
Gene: FXN HGNC NCBI

Linked Data

gnomAD v4: 9-69035708-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035708T>A , CM000671.2:g.69035708T>A GRCh38
NC_000009.11:g.71650624T>A , CM000671.1:g.71650624T>A GRCh37
NC_000009.10:g.70840444T>A NCBI36
NG_008845.2:g.5146T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377270.7:c.-75T>A ENSP00000366482.3:n.-75T>A
ENST00000396364.7:c.-75T>A ENSP00000379650.3:n.-75T>A
NM_000144.4:c.-75T>A NP_000135.2:n.-75T>A
NM_001161706.1:c.-75T>A NP_001155178.1:n.-75T>A
NM_181425.2:c.-75T>A NP_852090.1:n.-75T>A