Canonical Allele Identifier: CA752546049
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1242169012

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474970G>T , CM000684.2:g.32474970G>T GRCh38
NC_000022.10:g.32870957G>T , CM000684.1:g.32870957G>T GRCh37
NC_000022.9:g.31200957G>T NCBI36
NG_016001.1:g.5251G>T
NG_016001.2:g.5251G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-33G>T MANE Select ENSP00000266087.7:n.-33G>T
ENST00000266087.11:c.-33G>T ENSP00000266087.7:n.-33G>T
ENST00000420700.5:c.-33G>T ENSP00000406155.1:n.-33G>T
ENST00000425028.5:c.-33G>T ENSP00000395823.1:n.-33G>T
NM_012179.3:c.-33G>T NP_036311.3:n.-33G>T
XM_011530106.1:c.-206G>T XP_011528408.1:n.-206G>T
XM_024452207.1:c.-223G>T XP_024307975.1:n.-223G>T
NM_012179.4:c.-33G>T MANE Select NP_036311.3:n.-33G>T