Canonical Allele Identifier: CA752545681
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1450012741
gnomAD v4: 22-32474677-G-A
MyVariant Identifiers: chr22:g.32870664G>A (hg19) chr22:g.32474677G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474677G>A , CM000684.2:g.32474677G>A GRCh38
NC_000022.10:g.32870664G>A , CM000684.1:g.32870664G>A GRCh37
NC_000022.9:g.31200664G>A NCBI36
NG_016001.1:g.4958G>A
NG_016001.2:g.4958G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-326G>A ENSP00000266087.7:n.-326G>A
ENST00000420700.5:c.-326G>A ENSP00000406155.1:n.-326G>A
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