Canonical Allele Identifier: CA2656311086
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474702-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474702G>A , CM000684.2:g.32474702G>A GRCh38
NC_000022.10:g.32870689G>A , CM000684.1:g.32870689G>A GRCh37
NC_000022.9:g.31200689G>A NCBI36
NG_016001.1:g.4983G>A
NG_016001.2:g.4983G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-301G>A ENSP00000266087.7:n.-301G>A
ENST00000420700.5:c.-301G>A ENSP00000406155.1:n.-301G>A
XM_011530106.1:c.-474G>A XP_011528408.1:n.-474G>A
XM_024452207.1:c.-491G>A XP_024307975.1:n.-491G>A
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