Canonical Allele Identifier: CA323427829
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs886292968
gnomAD v2: 22-32870890-A-G
gnomAD v3: 22-32474903-A-G
gnomAD v4: 22-32474903-A-G
MyVariant Identifiers: chr22:g.32870890A>G (hg19) chr22:g.32474903A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474903A>G , CM000684.2:g.32474903A>G GRCh38
NC_000022.10:g.32870890A>G , CM000684.1:g.32870890A>G GRCh37
NC_000022.9:g.31200890A>G NCBI36
NG_016001.1:g.5184A>G
NG_016001.2:g.5184A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-100A>G MANE Select ENSP00000266087.7:n.-100A>G
ENST00000266087.11:c.-100A>G ENSP00000266087.7:n.-100A>G
ENST00000420700.5:c.-100A>G ENSP00000406155.1:n.-100A>G
ENST00000425028.5:c.-100A>G ENSP00000395823.1:n.-100A>G
NM_012179.3:c.-100A>G NP_036311.3:n.-100A>G
XM_011530106.1:c.-273A>G XP_011528408.1:n.-273A>G
XM_024452207.1:c.-290A>G XP_024307975.1:n.-290A>G
NM_012179.4:c.-100A>G MANE Select NP_036311.3:n.-100A>G
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