Canonical Allele Identifier: CA752545715
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1265375991
gnomAD v3: 22-32474727-G-A
gnomAD v4: 22-32474727-G-A
MyVariant Identifiers: chr22:g.32870714G>A (hg19) chr22:g.32474727G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474727G>A , CM000684.2:g.32474727G>A GRCh38
NC_000022.10:g.32870714G>A , CM000684.1:g.32870714G>A GRCh37
NC_000022.9:g.31200714G>A NCBI36
NG_016001.1:g.5008G>A
NG_016001.2:g.5008G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-276G>A ENSP00000266087.7:n.-276G>A
ENST00000420700.5:c.-276G>A ENSP00000406155.1:n.-276G>A
NM_012179.3:c.-276G>A NP_036311.3:n.-276G>A
XM_011530106.1:c.-449G>A XP_011528408.1:n.-449G>A
XM_024452207.1:c.-466G>A XP_024307975.1:n.-466G>A
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