Canonical Allele Identifier: CA514294407
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32475113-C-A
MyVariant Identifiers: chr22:g.32871100C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475113C>A , CM000684.2:g.32475113C>A GRCh38
NC_000022.10:g.32871100C>A , CM000684.1:g.32871100C>A GRCh37
NC_000022.9:g.31201100C>A NCBI36
NG_016001.1:g.5394C>A
NG_016001.2:g.5394C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.111C>A MANE Select ENSP00000266087.7:p.Thr37=
ENST00000266087.11:c.111C>A ENSP00000266087.7:p.Thr37=
ENST00000420700.5:c.111C>A ENSP00000406155.1:p.Thr37=
ENST00000425028.5:c.111C>A ENSP00000395823.1:p.Thr37=
ENST00000492535.1:n.99C>A
NM_012179.3:c.111C>A NP_036311.3:p.Thr37=
XM_011530106.1:c.-63C>A XP_011528408.1:n.-63C>A
XM_024452207.1:c.-80C>A XP_024307975.1:n.-80C>A
NM_012179.4:c.111C>A MANE Select NP_036311.3:p.Thr37=
Search 100 bp 5'
Search 100 bp 3'