Canonical Allele Identifier: CA942198242
Gene: FDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1946552643
gnomAD v3: 11-110460950-A-G
gnomAD v4: 11-110460950-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110460950A>G , CM000673.2:g.110460950A>G GRCh38
NC_000011.9:g.110331674A>G , CM000673.1:g.110331674A>G GRCh37
NC_000011.8:g.109836884A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260270.3:c.441-1404A>G MANE Select ENSP00000260270.2:n.441-1404A>G
ENST00000260270.2:c.441-1404A>G ENSP00000260270.2:n.441-1404A>G
NM_004109.4:c.441-1404A>G NP_004100.1:n.441-1404A>G
NM_004109.5:c.441-1404A>G MANE Select NP_004100.1:n.441-1404A>G
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