Canonical Allele Identifier: CA2656311384
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474912-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474912T>C , CM000684.2:g.32474912T>C GRCh38
NC_000022.10:g.32870899T>C , CM000684.1:g.32870899T>C GRCh37
NC_000022.9:g.31200899T>C NCBI36
NG_016001.1:g.5193T>C
NG_016001.2:g.5193T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-91T>C MANE Select ENSP00000266087.7:n.-91T>C
ENST00000266087.11:c.-91T>C ENSP00000266087.7:n.-91T>C
ENST00000420700.5:c.-91T>C ENSP00000406155.1:n.-91T>C
ENST00000425028.5:c.-91T>C ENSP00000395823.1:n.-91T>C
NM_012179.3:c.-91T>C NP_036311.3:n.-91T>C
XM_011530106.1:c.-264T>C XP_011528408.1:n.-264T>C
XM_024452207.1:c.-281T>C XP_024307975.1:n.-281T>C
NM_012179.4:c.-91T>C MANE Select NP_036311.3:n.-91T>C
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