Canonical Allele Identifier: CA411329839
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32475028-A-G
MyVariant Identifiers: chr22:g.32871015A>G (hg19) chr22:g.32475028A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475028A>G , CM000684.2:g.32475028A>G GRCh38
NC_000022.10:g.32871015A>G , CM000684.1:g.32871015A>G GRCh37
NC_000022.9:g.31201015A>G NCBI36
NG_016001.1:g.5309A>G
NG_016001.2:g.5309A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.26A>G MANE Select ENSP00000266087.7:p.Lys9Arg
ENST00000266087.11:c.26A>G ENSP00000266087.7:p.Lys9Arg
ENST00000420700.5:c.26A>G ENSP00000406155.1:p.Lys9Arg
ENST00000425028.5:c.26A>G ENSP00000395823.1:p.Lys9Arg
ENST00000492535.1:n.14A>G
NM_012179.3:c.26A>G NP_036311.3:p.Lys9Arg
XM_011530106.1:c.-148A>G XP_011528408.1:n.-148A>G
XM_024452207.1:c.-165A>G XP_024307975.1:n.-165A>G
NM_012179.4:c.26A>G MANE Select NP_036311.3:p.Lys9Arg
Search 100 bp 5'
Search 100 bp 3'