Canonical Allele Identifier: CA671631671
Gene: FDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1423161729
gnomAD v3: 11-110460972-A-C
gnomAD v4: 11-110460972-A-C
MyVariant Identifiers: chr11:g.110331696A>C (hg19) chr11:g.110460972A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110460972A>C , CM000673.2:g.110460972A>C GRCh38
NC_000011.9:g.110331696A>C , CM000673.1:g.110331696A>C GRCh37
NC_000011.8:g.109836906A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260270.3:c.441-1382A>C MANE Select ENSP00000260270.2:n.441-1382A>C
ENST00000260270.2:c.441-1382A>C ENSP00000260270.2:n.441-1382A>C
NM_004109.4:c.441-1382A>C NP_004100.1:n.441-1382A>C
NM_004109.5:c.441-1382A>C MANE Select NP_004100.1:n.441-1382A>C
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