Canonical Allele Identifier: CA323427684
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs763208669

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474689A>G , CM000684.2:g.32474689A>G GRCh38
NC_000022.10:g.32870676A>G , CM000684.1:g.32870676A>G GRCh37
NC_000022.9:g.31200676A>G NCBI36
NG_016001.1:g.4970A>G
NG_016001.2:g.4970A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-314A>G ENSP00000266087.7:n.-314A>G
ENST00000420700.5:c.-314A>G ENSP00000406155.1:n.-314A>G
XM_011530106.1:c.-487A>G XP_011528408.1:n.-487A>G
XM_024452207.1:c.-504A>G XP_024307975.1:n.-504A>G