Canonical Allele Identifier: CA2577697716
Gene: FBXO7 HGNC NCBI

Linked Data

gnomAD v4: 22-32474908-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474908G>T , CM000684.2:g.32474908G>T GRCh38
NC_000022.10:g.32870895G>T , CM000684.1:g.32870895G>T GRCh37
NC_000022.9:g.31200895G>T NCBI36
NG_016001.1:g.5189G>T
NG_016001.2:g.5189G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-95G>T MANE Select ENSP00000266087.7:n.-95G>T
ENST00000266087.11:c.-95G>T ENSP00000266087.7:n.-95G>T
ENST00000420700.5:c.-95G>T ENSP00000406155.1:n.-95G>T
ENST00000425028.5:c.-95G>T ENSP00000395823.1:n.-95G>T
NM_012179.3:c.-95G>T NP_036311.3:n.-95G>T
XM_011530106.1:c.-268G>T XP_011528408.1:n.-268G>T
XM_024452207.1:c.-285G>T XP_024307975.1:n.-285G>T
NM_012179.4:c.-95G>T MANE Select NP_036311.3:n.-95G>T
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