Canonical Allele Identifier: CA2401985179
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1402964126

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474989C>T , CM000684.2:g.32474989C>T GRCh38
NC_000022.10:g.32870976C>T , CM000684.1:g.32870976C>T GRCh37
NC_000022.9:g.31200976C>T NCBI36
NG_016001.1:g.5270C>T
NG_016001.2:g.5270C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-14C>T MANE Select ENSP00000266087.7:n.-14C>T
ENST00000266087.11:c.-14C>T ENSP00000266087.7:n.-14C>T
ENST00000420700.5:c.-14C>T ENSP00000406155.1:n.-14C>T
ENST00000425028.5:c.-14C>T ENSP00000395823.1:n.-14C>T
NM_012179.3:c.-14C>T NP_036311.3:n.-14C>T
XM_011530106.1:c.-187C>T XP_011528408.1:n.-187C>T
XM_024452207.1:c.-204C>T XP_024307975.1:n.-204C>T
NM_012179.4:c.-14C>T MANE Select NP_036311.3:n.-14C>T