Canonical Allele Identifier: CA2818776595
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474995C>G , CM000684.2:g.32474995C>G GRCh38
NC_000022.10:g.32870982C>G , CM000684.1:g.32870982C>G GRCh37
NC_000022.9:g.31200982C>G NCBI36
NG_016001.1:g.5276C>G
NG_016001.2:g.5276C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-8C>G MANE Select ENSP00000266087.7:n.-8C>G
ENST00000266087.11:c.-8C>G ENSP00000266087.7:n.-8C>G
ENST00000420700.5:c.-8C>G ENSP00000406155.1:n.-8C>G
ENST00000425028.5:c.-8C>G ENSP00000395823.1:n.-8C>G
NM_012179.3:c.-8C>G NP_036311.3:n.-8C>G
XM_011530106.1:c.-181C>G XP_011528408.1:n.-181C>G
XM_024452207.1:c.-198C>G XP_024307975.1:n.-198C>G
NM_012179.4:c.-8C>G MANE Select NP_036311.3:n.-8C>G