Canonical Allele Identifier: CA411329925
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871054C>G (hg19) chr22:g.32475067C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475067C>G , CM000684.2:g.32475067C>G GRCh38
NC_000022.10:g.32871054C>G , CM000684.1:g.32871054C>G GRCh37
NC_000022.9:g.31201054C>G NCBI36
NG_016001.1:g.5348C>G
NG_016001.2:g.5348C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.65C>G MANE Select ENSP00000266087.7:p.Thr22Arg
ENST00000266087.11:c.65C>G ENSP00000266087.7:p.Thr22Arg
ENST00000420700.5:c.65C>G ENSP00000406155.1:p.Thr22Arg
ENST00000425028.5:c.65C>G ENSP00000395823.1:p.Thr22Arg
ENST00000492535.1:n.53C>G
NM_012179.3:c.65C>G NP_036311.3:p.Thr22Arg
XM_011530106.1:c.-109C>G XP_011528408.1:n.-109C>G
XM_024452207.1:c.-126C>G XP_024307975.1:n.-126C>G
NM_012179.4:c.65C>G MANE Select NP_036311.3:p.Thr22Arg
Search 100 bp 5'
Search 100 bp 3'