Canonical Allele Identifier: CA2656311451
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474988-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474988C>T , CM000684.2:g.32474988C>T GRCh38
NC_000022.10:g.32870975C>T , CM000684.1:g.32870975C>T GRCh37
NC_000022.9:g.31200975C>T NCBI36
NG_016001.1:g.5269C>T
NG_016001.2:g.5269C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-15C>T MANE Select ENSP00000266087.7:n.-15C>T
ENST00000266087.11:c.-15C>T ENSP00000266087.7:n.-15C>T
ENST00000420700.5:c.-15C>T ENSP00000406155.1:n.-15C>T
ENST00000425028.5:c.-15C>T ENSP00000395823.1:n.-15C>T
NM_012179.3:c.-15C>T NP_036311.3:n.-15C>T
XM_011530106.1:c.-188C>T XP_011528408.1:n.-188C>T
XM_024452207.1:c.-205C>T XP_024307975.1:n.-205C>T
NM_012179.4:c.-15C>T MANE Select NP_036311.3:n.-15C>T
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