Canonical Allele Identifier: CA323427753
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1028425205
gnomAD v4: 22-32474785-G-C
MyVariant Identifiers: chr22:g.32870772G>C (hg19) chr22:g.32474785G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474785G>C , CM000684.2:g.32474785G>C GRCh38
NC_000022.10:g.32870772G>C , CM000684.1:g.32870772G>C GRCh37
NC_000022.9:g.31200772G>C NCBI36
NG_016001.1:g.5066G>C
NG_016001.2:g.5066G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-218G>C ENSP00000266087.7:n.-218G>C
ENST00000420700.5:c.-218G>C ENSP00000406155.1:n.-218G>C
NM_012179.3:c.-218G>C NP_036311.3:n.-218G>C
XM_011530106.1:c.-391G>C XP_011528408.1:n.-391G>C
XM_024452207.1:c.-408G>C XP_024307975.1:n.-408G>C
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