Canonical Allele Identifier: CA323427860
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1049916705
gnomAD v2: 22-32870934-CCGCCGTCCCCGT-C
gnomAD v3: 22-32474947-CCGCCGTCCCCGT-C
gnomAD v4: 22-32474947-CCGCCGTCCCCGT-C
MyVariant Identifiers: chr22:g.32870935_32870946del (hg19) chr22:g.32474948_32474959del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474953_32474964del , CM000684.2:g.32474953_32474964del GRCh38
NC_000022.10:g.32870940_32870951del , CM000684.1:g.32870940_32870951del GRCh37
NC_000022.9:g.31200940_31200951del NCBI36
NG_016001.1:g.5234_5245del
NG_016001.2:g.5234_5245del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-50_-39del MANE Select ENSP00000266087.7:n.-50_-39del
ENST00000266087.11:c.-50_-39del ENSP00000266087.7:n.-50_-39del
ENST00000420700.5:c.-50_-39del ENSP00000406155.1:n.-50_-39del
ENST00000425028.5:c.-50_-39del ENSP00000395823.1:n.-50_-39del
NM_012179.3:c.-50_-39del NP_036311.3:n.-50_-39del
XM_011530106.1:c.-223_-212del XP_011528408.1:n.-223_-212del
XM_024452207.1:c.-240_-229del XP_024307975.1:n.-240_-229del
NM_012179.4:c.-50_-39del MANE Select NP_036311.3:n.-50_-39del
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