Canonical Allele Identifier: CA229042121
Gene: FDX1 HGNC NCBI

Linked Data

dbSNP Id: rs897256973
gnomAD v3: 11-110460882-A-G
gnomAD v4: 11-110460882-A-G
MyVariant Identifiers: chr11:g.110331606A>G (hg19) chr11:g.110460882A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110460882A>G , CM000673.2:g.110460882A>G GRCh38
NC_000011.9:g.110331606A>G , CM000673.1:g.110331606A>G GRCh37
NC_000011.8:g.109836816A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260270.3:c.441-1472A>G MANE Select ENSP00000260270.2:n.441-1472A>G
ENST00000260270.2:c.441-1472A>G ENSP00000260270.2:n.441-1472A>G
NM_004109.4:c.441-1472A>G NP_004100.1:n.441-1472A>G
NM_004109.5:c.441-1472A>G MANE Select NP_004100.1:n.441-1472A>G
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