Canonical Allele Identifier: CA2690187548
Gene: FXN HGNC NCBI

Linked Data

gnomAD v4: 9-69035688-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035688C>T , CM000671.2:g.69035688C>T GRCh38
NC_000009.11:g.71650604C>T , CM000671.1:g.71650604C>T GRCh37
NC_000009.10:g.70840424C>T NCBI36
NG_008845.2:g.5126C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-95C>T ENSP00000366482.3:n.-95C>T
ENST00000396364.7:c.-95C>T ENSP00000379650.3:n.-95C>T
NM_000144.4:c.-95C>T NP_000135.2:n.-95C>T
NM_001161706.1:c.-95C>T NP_001155178.1:n.-95C>T
NM_181425.2:c.-95C>T NP_852090.1:n.-95C>T