Canonical Allele Identifier: CA2656311421
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474950-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474950C>G , CM000684.2:g.32474950C>G GRCh38
NC_000022.10:g.32870937C>G , CM000684.1:g.32870937C>G GRCh37
NC_000022.9:g.31200937C>G NCBI36
NG_016001.1:g.5231C>G
NG_016001.2:g.5231C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-53C>G MANE Select ENSP00000266087.7:n.-53C>G
ENST00000266087.11:c.-53C>G ENSP00000266087.7:n.-53C>G
ENST00000420700.5:c.-53C>G ENSP00000406155.1:n.-53C>G
ENST00000425028.5:c.-53C>G ENSP00000395823.1:n.-53C>G
NM_012179.3:c.-53C>G NP_036311.3:n.-53C>G
XM_011530106.1:c.-226C>G XP_011528408.1:n.-226C>G
XM_024452207.1:c.-243C>G XP_024307975.1:n.-243C>G
NM_012179.4:c.-53C>G MANE Select NP_036311.3:n.-53C>G
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