Canonical Allele Identifier: CA514294323
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871031G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475044G>C , CM000684.2:g.32475044G>C GRCh38
NC_000022.10:g.32871031G>C , CM000684.1:g.32871031G>C GRCh37
NC_000022.9:g.31201031G>C NCBI36
NG_016001.1:g.5325G>C
NG_016001.2:g.5325G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.42G>C MANE Select ENSP00000266087.7:p.Leu14=
ENST00000266087.11:c.42G>C ENSP00000266087.7:p.Leu14=
ENST00000420700.5:c.42G>C ENSP00000406155.1:p.Leu14=
ENST00000425028.5:c.42G>C ENSP00000395823.1:p.Leu14=
ENST00000492535.1:n.30G>C
NM_012179.3:c.42G>C NP_036311.3:p.Leu14=
XM_011530106.1:c.-132G>C XP_011528408.1:n.-132G>C
XM_024452207.1:c.-149G>C XP_024307975.1:n.-149G>C
NM_012179.4:c.42G>C MANE Select NP_036311.3:p.Leu14=
Search 100 bp 5'
Search 100 bp 3'