Canonical Allele Identifier: CA1025186125
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1260610835

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474694C>G , CM000684.2:g.32474694C>G GRCh38
NC_000022.10:g.32870681C>G , CM000684.1:g.32870681C>G GRCh37
NC_000022.9:g.31200681C>G NCBI36
NG_016001.1:g.4975C>G
NG_016001.2:g.4975C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-309C>G ENSP00000266087.7:n.-309C>G
ENST00000420700.5:c.-309C>G ENSP00000406155.1:n.-309C>G
XM_011530106.1:c.-482C>G XP_011528408.1:n.-482C>G
XM_024452207.1:c.-499C>G XP_024307975.1:n.-499C>G