Canonical Allele Identifier: CA323427930
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs920292109

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475064C>T , CM000684.2:g.32475064C>T GRCh38
NC_000022.10:g.32871051C>T , CM000684.1:g.32871051C>T GRCh37
NC_000022.9:g.31201051C>T NCBI36
NG_016001.1:g.5345C>T
NG_016001.2:g.5345C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.62C>T MANE Select ENSP00000266087.7:p.Pro21Leu
ENST00000266087.11:c.62C>T ENSP00000266087.7:p.Pro21Leu
ENST00000420700.5:c.62C>T ENSP00000406155.1:p.Pro21Leu
ENST00000425028.5:c.62C>T ENSP00000395823.1:p.Pro21Leu
ENST00000492535.1:n.50C>T
NM_012179.3:c.62C>T NP_036311.3:p.Pro21Leu
XM_011530106.1:c.-112C>T XP_011528408.1:n.-112C>T
XM_024452207.1:c.-129C>T XP_024307975.1:n.-129C>T
NM_012179.4:c.62C>T MANE Select NP_036311.3:p.Pro21Leu