Canonical Allele Identifier: CA323427685
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs968653534

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474697T>G , CM000684.2:g.32474697T>G GRCh38
NC_000022.10:g.32870684T>G , CM000684.1:g.32870684T>G GRCh37
NC_000022.9:g.31200684T>G NCBI36
NG_016001.1:g.4978T>G
NG_016001.2:g.4978T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-306T>G ENSP00000266087.7:n.-306T>G
ENST00000420700.5:c.-306T>G ENSP00000406155.1:n.-306T>G
XM_011530106.1:c.-479T>G XP_011528408.1:n.-479T>G
XM_024452207.1:c.-496T>G XP_024307975.1:n.-496T>G