Canonical Allele Identifier: CA2690187488

Gene: FXN

Linked Data

• gnomAD v4: 9-69035619-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69035619C>G , CM000671.2:g.69035619C>G	GRCh38
NC_000009.11:g.71650535C>G , CM000671.1:g.71650535C>G	GRCh37
NC_000009.10:g.70840355C>G	NCBI36
NG_008845.2:g.5057C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.7:c.-164C>G	ENSP00000366482.3:n.-164C>G
ENST00000396364.7:c.-164C>G	ENSP00000379650.3:n.-164C>G
NM_000144.4:c.-164C>G	NP_000135.2:n.-164C>G
NM_001161706.1:c.-164C>G	NP_001155178.1:n.-164C>G
NM_181425.2:c.-164C>G	NP_852090.1:n.-164C>G