Canonical Allele Identifier: CA10201287
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs756104854

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474980C>T , CM000684.2:g.32474980C>T GRCh38
NC_000022.10:g.32870967C>T , CM000684.1:g.32870967C>T GRCh37
NC_000022.9:g.31200967C>T NCBI36
NG_016001.1:g.5261C>T
NG_016001.2:g.5261C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-23C>T MANE Select ENSP00000266087.7:n.-23C>T
ENST00000266087.11:c.-23C>T ENSP00000266087.7:n.-23C>T
ENST00000420700.5:c.-23C>T ENSP00000406155.1:n.-23C>T
ENST00000425028.5:c.-23C>T ENSP00000395823.1:n.-23C>T
NM_012179.3:c.-23C>T NP_036311.3:n.-23C>T
XM_011530106.1:c.-196C>T XP_011528408.1:n.-196C>T
XM_024452207.1:c.-213C>T XP_024307975.1:n.-213C>T
NM_012179.4:c.-23C>T MANE Select NP_036311.3:n.-23C>T