Canonical Allele Identifier: CA411329949
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871066T>G (hg19) chr22:g.32475079T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475079T>G , CM000684.2:g.32475079T>G GRCh38
NC_000022.10:g.32871066T>G , CM000684.1:g.32871066T>G GRCh37
NC_000022.9:g.31201066T>G NCBI36
NG_016001.1:g.5360T>G
NG_016001.2:g.5360T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.77T>G MANE Select ENSP00000266087.7:p.Leu26Trp
ENST00000266087.11:c.77T>G ENSP00000266087.7:p.Leu26Trp
ENST00000420700.5:c.77T>G ENSP00000406155.1:p.Leu26Trp
ENST00000425028.5:c.77T>G ENSP00000395823.1:p.Leu26Trp
ENST00000492535.1:n.65T>G
NM_012179.3:c.77T>G NP_036311.3:p.Leu26Trp
XM_011530106.1:c.-97T>G XP_011528408.1:n.-97T>G
XM_024452207.1:c.-114T>G XP_024307975.1:n.-114T>G
NM_012179.4:c.77T>G MANE Select NP_036311.3:p.Leu26Trp
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