Canonical Allele Identifier: CA193368758
Gene: FXN HGNC NCBI

Linked Data

dbSNP Id: rs536839594
gnomAD v2: 9-71650607-C-T
gnomAD v3: 9-69035691-C-T
gnomAD v4: 9-69035691-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035691C>T , CM000671.2:g.69035691C>T GRCh38
NC_000009.11:g.71650607C>T , CM000671.1:g.71650607C>T GRCh37
NC_000009.10:g.70840427C>T NCBI36
NG_008845.2:g.5129C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-92C>T ENSP00000366482.3:n.-92C>T
ENST00000396364.7:c.-92C>T ENSP00000379650.3:n.-92C>T
NM_000144.4:c.-92C>T NP_000135.2:n.-92C>T
NM_001161706.1:c.-92C>T NP_001155178.1:n.-92C>T
NM_181425.2:c.-92C>T NP_852090.1:n.-92C>T