Canonical Allele Identifier: CA1025186420
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs2057416298

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474979C>T , CM000684.2:g.32474979C>T GRCh38
NC_000022.10:g.32870966C>T , CM000684.1:g.32870966C>T GRCh37
NC_000022.9:g.31200966C>T NCBI36
NG_016001.1:g.5260C>T
NG_016001.2:g.5260C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-24C>T MANE Select ENSP00000266087.7:n.-24C>T
ENST00000266087.11:c.-24C>T ENSP00000266087.7:n.-24C>T
ENST00000420700.5:c.-24C>T ENSP00000406155.1:n.-24C>T
ENST00000425028.5:c.-24C>T ENSP00000395823.1:n.-24C>T
NM_012179.3:c.-24C>T NP_036311.3:n.-24C>T
XM_011530106.1:c.-197C>T XP_011528408.1:n.-197C>T
XM_024452207.1:c.-214C>T XP_024307975.1:n.-214C>T
NM_012179.4:c.-24C>T MANE Select NP_036311.3:n.-24C>T