Canonical Allele Identifier: CA2690187481
Gene: FXN HGNC NCBI

Linked Data

gnomAD v4: 9-69035611-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035611A>C , CM000671.2:g.69035611A>C GRCh38
NC_000009.11:g.71650527A>C , CM000671.1:g.71650527A>C GRCh37
NC_000009.10:g.70840347A>C NCBI36
NG_008845.2:g.5049A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-172A>C ENSP00000366482.3:n.-172A>C
ENST00000396364.7:c.-172A>C ENSP00000379650.3:n.-172A>C
NM_000144.4:c.-172A>C NP_000135.2:n.-172A>C
NM_001161706.1:c.-172A>C NP_001155178.1:n.-172A>C
NM_181425.2:c.-172A>C NP_852090.1:n.-172A>C
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