Canonical Allele Identifier: CA193368759
Gene: FXN HGNC NCBI

Linked Data

dbSNP Id: rs971280020
gnomAD v4: 9-69035697-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035697A>G , CM000671.2:g.69035697A>G GRCh38
NC_000009.11:g.71650613A>G , CM000671.1:g.71650613A>G GRCh37
NC_000009.10:g.70840433A>G NCBI36
NG_008845.2:g.5135A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-86A>G ENSP00000366482.3:n.-86A>G
ENST00000396364.7:c.-86A>G ENSP00000379650.3:n.-86A>G
NM_000144.4:c.-86A>G NP_000135.2:n.-86A>G
NM_001161706.1:c.-86A>G NP_001155178.1:n.-86A>G
NM_181425.2:c.-86A>G NP_852090.1:n.-86A>G