Canonical Allele Identifier: CA2690187478

Gene: FXN

Linked Data

• gnomAD v4: 9-69035607-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69035607A>G , CM000671.2:g.69035607A>G	GRCh38
NC_000009.11:g.71650523A>G , CM000671.1:g.71650523A>G	GRCh37
NC_000009.10:g.70840343A>G	NCBI36
NG_008845.2:g.5045A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377270.7:c.-176A>G	ENSP00000366482.3:n.-176A>G
ENST00000396364.7:c.-176A>G	ENSP00000379650.3:n.-176A>G
NM_000144.4:c.-176A>G	NP_000135.2:n.-176A>G
NM_001161706.1:c.-176A>G	NP_001155178.1:n.-176A>G
NM_181425.2:c.-176A>G	NP_852090.1:n.-176A>G