Canonical Allele Identifier: CA411329952
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871068C>A (hg19) chr22:g.32475081C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475081C>A , CM000684.2:g.32475081C>A GRCh38
NC_000022.10:g.32871068C>A , CM000684.1:g.32871068C>A GRCh37
NC_000022.9:g.31201068C>A NCBI36
NG_016001.1:g.5362C>A
NG_016001.2:g.5362C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.79C>A MANE Select ENSP00000266087.7:p.Arg27Ser
ENST00000266087.11:c.79C>A ENSP00000266087.7:p.Arg27Ser
ENST00000420700.5:c.79C>A ENSP00000406155.1:p.Arg27Ser
ENST00000425028.5:c.79C>A ENSP00000395823.1:p.Arg27Ser
ENST00000492535.1:n.67C>A
NM_012179.3:c.79C>A NP_036311.3:p.Arg27Ser
XM_011530106.1:c.-95C>A XP_011528408.1:n.-95C>A
XM_024452207.1:c.-112C>A XP_024307975.1:n.-112C>A
NM_012179.4:c.79C>A MANE Select NP_036311.3:p.Arg27Ser
Search 100 bp 5'
Search 100 bp 3'