Canonical Allele Identifier: CA514294364
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871056C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475069C>T , CM000684.2:g.32475069C>T GRCh38
NC_000022.10:g.32871056C>T , CM000684.1:g.32871056C>T GRCh37
NC_000022.9:g.31201056C>T NCBI36
NG_016001.1:g.5350C>T
NG_016001.2:g.5350C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.67C>T MANE Select ENSP00000266087.7:p.Leu23=
ENST00000266087.11:c.67C>T ENSP00000266087.7:p.Leu23=
ENST00000420700.5:c.67C>T ENSP00000406155.1:p.Leu23=
ENST00000425028.5:c.67C>T ENSP00000395823.1:p.Leu23=
ENST00000492535.1:n.55C>T
NM_012179.3:c.67C>T NP_036311.3:p.Leu23=
XM_011530106.1:c.-107C>T XP_011528408.1:n.-107C>T
XM_024452207.1:c.-124C>T XP_024307975.1:n.-124C>T
NM_012179.4:c.67C>T MANE Select NP_036311.3:p.Leu23=