Canonical Allele Identifier: CA866340051

Gene: FXN

Linked Data

• dbSNP Id: rs1488269824
• gnomAD v3: 9-69035616-G-T
• gnomAD v4: 9-69035616-G-T
• MyVariant Identifiers: chr9:g.71650532G>T (hg19) ; chr9:g.69035616G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69035616G>T , CM000671.2:g.69035616G>T	GRCh38
NC_000009.11:g.71650532G>T , CM000671.1:g.71650532G>T	GRCh37
NC_000009.10:g.70840352G>T	NCBI36
NG_008845.2:g.5054G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377270.7:c.-167G>T	ENSP00000366482.3:n.-167G>T
ENST00000396364.7:c.-167G>T	ENSP00000379650.3:n.-167G>T
NM_000144.4:c.-167G>T	NP_000135.2:n.-167G>T
NM_001161706.1:c.-167G>T	NP_001155178.1:n.-167G>T
NM_181425.2:c.-167G>T	NP_852090.1:n.-167G>T