Canonical Allele Identifier: CA323427734
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs560375108
gnomAD v3: 22-32474762-C-T
gnomAD v4: 22-32474762-C-T
MyVariant Identifiers: chr22:g.32870749C>T (hg19) chr22:g.32474762C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474762C>T , CM000684.2:g.32474762C>T GRCh38
NC_000022.10:g.32870749C>T , CM000684.1:g.32870749C>T GRCh37
NC_000022.9:g.31200749C>T NCBI36
NG_016001.1:g.5043C>T
NG_016001.2:g.5043C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.11:c.-241C>T ENSP00000266087.7:n.-241C>T
ENST00000420700.5:c.-241C>T ENSP00000406155.1:n.-241C>T
NM_012179.3:c.-241C>T NP_036311.3:n.-241C>T
XM_011530106.1:c.-414C>T XP_011528408.1:n.-414C>T
XM_024452207.1:c.-431C>T XP_024307975.1:n.-431C>T
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