Canonical Allele Identifier: CA411329829
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871009T>C (hg19) chr22:g.32475022T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475022T>C , CM000684.2:g.32475022T>C GRCh38
NC_000022.10:g.32871009T>C , CM000684.1:g.32871009T>C GRCh37
NC_000022.9:g.31201009T>C NCBI36
NG_016001.1:g.5303T>C
NG_016001.2:g.5303T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.20T>C MANE Select ENSP00000266087.7:p.Leu7Pro
ENST00000266087.11:c.20T>C ENSP00000266087.7:p.Leu7Pro
ENST00000420700.5:c.20T>C ENSP00000406155.1:p.Leu7Pro
ENST00000425028.5:c.20T>C ENSP00000395823.1:p.Leu7Pro
ENST00000492535.1:n.8T>C
NM_012179.3:c.20T>C NP_036311.3:p.Leu7Pro
XM_011530106.1:c.-154T>C XP_011528408.1:n.-154T>C
XM_024452207.1:c.-171T>C XP_024307975.1:n.-171T>C
NM_012179.4:c.20T>C MANE Select NP_036311.3:p.Leu7Pro
Search 100 bp 5'
Search 100 bp 3'