Canonical Allele Identifier: CA2589928402
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475161T>G , CM000684.2:g.32475161T>G GRCh38
NC_000022.10:g.32871148T>G , CM000684.1:g.32871148T>G GRCh37
NC_000022.9:g.31201148T>G NCBI36
NG_016001.1:g.5442T>G
NG_016001.2:g.5442T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.122+37T>G MANE Select ENSP00000266087.7:n.122+37T>G
ENST00000266087.11:c.122+37T>G ENSP00000266087.7:n.122+37T>G
ENST00000420700.5:c.122+37T>G ENSP00000406155.1:n.122+37T>G
ENST00000425028.5:c.122+37T>G ENSP00000395823.1:n.122+37T>G
ENST00000492535.1:n.110+37T>G
NM_012179.3:c.122+37T>G NP_036311.3:n.122+37T>G
XM_011530106.1:c.-52+37T>G XP_011528408.1:n.-52+37T>G
XM_024452207.1:c.-69+37T>G XP_024307975.1:n.-69+37T>G
NM_012179.4:c.122+37T>G MANE Select NP_036311.3:n.122+37T>G