Canonical Allele Identifier: CA1854034811
Gene: FXN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035597C= , CM000671.2:g.69035597C= GRCh38
NC_000009.11:g.71650513C= , CM000671.1:g.71650513C= GRCh37
NC_000009.10:g.70840333C= NCBI36
NG_008845.2:g.5035C=

Transcript Alleles

HGVS Amino-acid change
ENST00000377270.7:c.-186C= ENSP00000366482.3:n.-186C=
ENST00000396364.7:c.-186C= ENSP00000379650.3:n.-186C=
NM_000144.4:c.-186C= NP_000135.2:n.-186C=
NM_001161706.1:c.-186C= NP_001155178.1:n.-186C=
NM_181425.2:c.-186C= NP_852090.1:n.-186C=