Canonical Allele Identifier: CA514294256
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32475011-G-A
MyVariant Identifiers: chr22:g.32870998G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475011G>A , CM000684.2:g.32475011G>A GRCh38
NC_000022.10:g.32870998G>A , CM000684.1:g.32870998G>A GRCh37
NC_000022.9:g.31200998G>A NCBI36
NG_016001.1:g.5292G>A
NG_016001.2:g.5292G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.9G>A MANE Select ENSP00000266087.7:p.Leu3=
ENST00000266087.11:c.9G>A ENSP00000266087.7:p.Leu3=
ENST00000420700.5:c.9G>A ENSP00000406155.1:p.Leu3=
ENST00000425028.5:c.9G>A ENSP00000395823.1:p.Leu3=
NM_012179.3:c.9G>A NP_036311.3:p.Leu3=
XM_011530106.1:c.-165G>A XP_011528408.1:n.-165G>A
XM_024452207.1:c.-182G>A XP_024307975.1:n.-182G>A
NM_012179.4:c.9G>A MANE Select NP_036311.3:p.Leu3=
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Search 100 bp 3'