Canonical Allele Identifier: CA2656311444
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474982-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474982C>A , CM000684.2:g.32474982C>A GRCh38
NC_000022.10:g.32870969C>A , CM000684.1:g.32870969C>A GRCh37
NC_000022.9:g.31200969C>A NCBI36
NG_016001.1:g.5263C>A
NG_016001.2:g.5263C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-21C>A MANE Select ENSP00000266087.7:n.-21C>A
ENST00000266087.11:c.-21C>A ENSP00000266087.7:n.-21C>A
ENST00000420700.5:c.-21C>A ENSP00000406155.1:n.-21C>A
ENST00000425028.5:c.-21C>A ENSP00000395823.1:n.-21C>A
NM_012179.3:c.-21C>A NP_036311.3:n.-21C>A
XM_011530106.1:c.-194C>A XP_011528408.1:n.-194C>A
XM_024452207.1:c.-211C>A XP_024307975.1:n.-211C>A
NM_012179.4:c.-21C>A MANE Select NP_036311.3:n.-21C>A
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