Canonical Allele Identifier: CA323427714
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1044183502
MyVariant Identifiers: chr22:g.32870721C>A (hg19) chr22:g.32474734C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474734C>A , CM000684.2:g.32474734C>A GRCh38
NC_000022.10:g.32870721C>A , CM000684.1:g.32870721C>A GRCh37
NC_000022.9:g.31200721C>A NCBI36
NG_016001.1:g.5015C>A
NG_016001.2:g.5015C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-269C>A ENSP00000266087.7:n.-269C>A
ENST00000420700.5:c.-269C>A ENSP00000406155.1:n.-269C>A
NM_012179.3:c.-269C>A NP_036311.3:n.-269C>A
XM_011530106.1:c.-442C>A XP_011528408.1:n.-442C>A
XM_024452207.1:c.-459C>A XP_024307975.1:n.-459C>A
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