Canonical Allele Identifier: CA323427852
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs963886500
gnomAD v2: 22-32870916-G-A
gnomAD v3: 22-32474929-G-A
gnomAD v4: 22-32474929-G-A
MyVariant Identifiers: chr22:g.32870916G>A (hg19) chr22:g.32474929G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474929G>A , CM000684.2:g.32474929G>A GRCh38
NC_000022.10:g.32870916G>A , CM000684.1:g.32870916G>A GRCh37
NC_000022.9:g.31200916G>A NCBI36
NG_016001.1:g.5210G>A
NG_016001.2:g.5210G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-74G>A MANE Select ENSP00000266087.7:n.-74G>A
ENST00000266087.11:c.-74G>A ENSP00000266087.7:n.-74G>A
ENST00000420700.5:c.-74G>A ENSP00000406155.1:n.-74G>A
ENST00000425028.5:c.-74G>A ENSP00000395823.1:n.-74G>A
NM_012179.3:c.-74G>A NP_036311.3:n.-74G>A
XM_011530106.1:c.-247G>A XP_011528408.1:n.-247G>A
XM_024452207.1:c.-264G>A XP_024307975.1:n.-264G>A
NM_012179.4:c.-74G>A MANE Select NP_036311.3:n.-74G>A
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