Canonical Allele Identifier: CA671631595
Gene: FDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1427841847
MyVariant Identifiers: chr11:g.110331560G>T (hg19) chr11:g.110460836G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.110460836G>T , CM000673.2:g.110460836G>T GRCh38
NC_000011.9:g.110331560G>T , CM000673.1:g.110331560G>T GRCh37
NC_000011.8:g.109836770G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260270.3:c.441-1518G>T MANE Select ENSP00000260270.2:n.441-1518G>T
ENST00000260270.2:c.441-1518G>T ENSP00000260270.2:n.441-1518G>T
NM_004109.4:c.441-1518G>T NP_004100.1:n.441-1518G>T
NM_004109.5:c.441-1518G>T MANE Select NP_004100.1:n.441-1518G>T
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