Canonical Allele Identifier: CA229042132

Gene: FDX1

Linked Data

• dbSNP Id: rs535115816
• gnomAD v3: 11-110460965-G-A
• gnomAD v4: 11-110460965-G-A
• MyVariant Identifiers: chr11:g.110331689G>A (hg19) ; chr11:g.110460965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110460965G>A , CM000673.2:g.110460965G>A	GRCh38
NC_000011.9:g.110331689G>A , CM000673.1:g.110331689G>A	GRCh37
NC_000011.8:g.109836899G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260270.3:c.441-1389G>A MANE Select	ENSP00000260270.2:n.441-1389G>A
ENST00000260270.2:c.441-1389G>A	ENSP00000260270.2:n.441-1389G>A
NM_004109.4:c.441-1389G>A	NP_004100.1:n.441-1389G>A
NM_004109.5:c.441-1389G>A MANE Select	NP_004100.1:n.441-1389G>A