Canonical Allele Identifier: CA1025186133
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs2057413368
gnomAD v3: 22-32474696-T-G
gnomAD v4: 22-32474696-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474696T>G , CM000684.2:g.32474696T>G GRCh38
NC_000022.10:g.32870683T>G , CM000684.1:g.32870683T>G GRCh37
NC_000022.9:g.31200683T>G NCBI36
NG_016001.1:g.4977T>G
NG_016001.2:g.4977T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-307T>G ENSP00000266087.7:n.-307T>G
ENST00000420700.5:c.-307T>G ENSP00000406155.1:n.-307T>G
XM_011530106.1:c.-480T>G XP_011528408.1:n.-480T>G
XM_024452207.1:c.-497T>G XP_024307975.1:n.-497T>G
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