Canonical Allele Identifier: CA2656311059
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474676-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474676C>T , CM000684.2:g.32474676C>T GRCh38
NC_000022.10:g.32870663C>T , CM000684.1:g.32870663C>T GRCh37
NC_000022.9:g.31200663C>T NCBI36
NG_016001.1:g.4957C>T
NG_016001.2:g.4957C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-327C>T ENSP00000266087.7:n.-327C>T
ENST00000420700.5:c.-327C>T ENSP00000406155.1:n.-327C>T
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