Canonical Allele Identifier: CA2401985170
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs2057416276

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474976A>T , CM000684.2:g.32474976A>T GRCh38
NC_000022.10:g.32870963A>T , CM000684.1:g.32870963A>T GRCh37
NC_000022.9:g.31200963A>T NCBI36
NG_016001.1:g.5257A>T
NG_016001.2:g.5257A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-27A>T MANE Select ENSP00000266087.7:n.-27A>T
ENST00000266087.11:c.-27A>T ENSP00000266087.7:n.-27A>T
ENST00000420700.5:c.-27A>T ENSP00000406155.1:n.-27A>T
ENST00000425028.5:c.-27A>T ENSP00000395823.1:n.-27A>T
NM_012179.3:c.-27A>T NP_036311.3:n.-27A>T
XM_011530106.1:c.-200A>T XP_011528408.1:n.-200A>T
XM_024452207.1:c.-217A>T XP_024307975.1:n.-217A>T
NM_012179.4:c.-27A>T MANE Select NP_036311.3:n.-27A>T