Canonical Allele Identifier: CA323427687
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs979101054
gnomAD v4: 22-32474706-A-C
MyVariant Identifiers: chr22:g.32870693A>C (hg19) chr22:g.32474706A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474706A>C , CM000684.2:g.32474706A>C GRCh38
NC_000022.10:g.32870693A>C , CM000684.1:g.32870693A>C GRCh37
NC_000022.9:g.31200693A>C NCBI36
NG_016001.1:g.4987A>C
NG_016001.2:g.4987A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-297A>C ENSP00000266087.7:n.-297A>C
ENST00000420700.5:c.-297A>C ENSP00000406155.1:n.-297A>C
XM_011530106.1:c.-470A>C XP_011528408.1:n.-470A>C
XM_024452207.1:c.-487A>C XP_024307975.1:n.-487A>C
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