Canonical Allele Identifier: CA639098926
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs937602255
gnomAD v2: 22-32870959-G-C
gnomAD v4: 22-32474972-G-C
MyVariant Identifiers: chr22:g.32870959G>C (hg19) chr22:g.32474972G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474972G>C , CM000684.2:g.32474972G>C GRCh38
NC_000022.10:g.32870959G>C , CM000684.1:g.32870959G>C GRCh37
NC_000022.9:g.31200959G>C NCBI36
NG_016001.1:g.5253G>C
NG_016001.2:g.5253G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-31G>C MANE Select ENSP00000266087.7:n.-31G>C
ENST00000266087.11:c.-31G>C ENSP00000266087.7:n.-31G>C
ENST00000420700.5:c.-31G>C ENSP00000406155.1:n.-31G>C
ENST00000425028.5:c.-31G>C ENSP00000395823.1:n.-31G>C
NM_012179.3:c.-31G>C NP_036311.3:n.-31G>C
XM_011530106.1:c.-204G>C XP_011528408.1:n.-204G>C
XM_024452207.1:c.-221G>C XP_024307975.1:n.-221G>C
NM_012179.4:c.-31G>C MANE Select NP_036311.3:n.-31G>C
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