Canonical Allele Identifier: CA514294396
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871088C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475101C>G , CM000684.2:g.32475101C>G GRCh38
NC_000022.10:g.32871088C>G , CM000684.1:g.32871088C>G GRCh37
NC_000022.9:g.31201088C>G NCBI36
NG_016001.1:g.5382C>G
NG_016001.2:g.5382C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.99C>G MANE Select ENSP00000266087.7:p.Ser33=
ENST00000266087.11:c.99C>G ENSP00000266087.7:p.Ser33=
ENST00000420700.5:c.99C>G ENSP00000406155.1:p.Ser33=
ENST00000425028.5:c.99C>G ENSP00000395823.1:p.Ser33=
ENST00000492535.1:n.87C>G
NM_012179.3:c.99C>G NP_036311.3:p.Ser33=
XM_011530106.1:c.-75C>G XP_011528408.1:n.-75C>G
XM_024452207.1:c.-92C>G XP_024307975.1:n.-92C>G
NM_012179.4:c.99C>G MANE Select NP_036311.3:p.Ser33=
Search 100 bp 5'
Search 100 bp 3'