Canonical Allele Identifier: CA411329956
Gene: FBXO7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.32871069G>C (hg19) chr22:g.32475082G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475082G>C , CM000684.2:g.32475082G>C GRCh38
NC_000022.10:g.32871069G>C , CM000684.1:g.32871069G>C GRCh37
NC_000022.9:g.31201069G>C NCBI36
NG_016001.1:g.5363G>C
NG_016001.2:g.5363G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.80G>C MANE Select ENSP00000266087.7:p.Arg27Pro
ENST00000266087.11:c.80G>C ENSP00000266087.7:p.Arg27Pro
ENST00000420700.5:c.80G>C ENSP00000406155.1:p.Arg27Pro
ENST00000425028.5:c.80G>C ENSP00000395823.1:p.Arg27Pro
ENST00000492535.1:n.68G>C
NM_012179.3:c.80G>C NP_036311.3:p.Arg27Pro
XM_011530106.1:c.-94G>C XP_011528408.1:n.-94G>C
XM_024452207.1:c.-111G>C XP_024307975.1:n.-111G>C
NM_012179.4:c.80G>C MANE Select NP_036311.3:p.Arg27Pro
Search 100 bp 5'
Search 100 bp 3'