Canonical Allele Identifier: CA980196553
Gene: FBXO31 HGNC NCBI

Linked Data

dbSNP Id: rs533793773
gnomAD v3: 16-87331052-G-T
gnomAD v4: 16-87331052-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87331052G>T , CM000678.2:g.87331052G>T GRCh38
NC_000016.9:g.87364658G>T , CM000678.1:g.87364658G>T GRCh37
NC_000016.8:g.85922159G>T NCBI36
NG_047196.1:g.66056C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000636077.2:c.*236C>A ENSP00000490402.2:n.*236C>A
ENST00000311635.12:c.*236C>A MANE Select ENSP00000310841.4:n.*236C>A
ENST00000618298.6:c.*236C>A ENSP00000479703.1:n.*236C>A
ENST00000311635.11:c.*236C>A ENSP00000310841.4:n.*236C>A
ENST00000565593.1:c.*562C>A ENSP00000455772.1:n.*562C>A
ENST00000568879.1:c.388+2834C>A
ENST00000618298.4:c.*236C>A ENSP00000479703.1:n.*236C>A
NM_001282683.1:c.*236C>A NP_001269612.1:n.*236C>A
NM_024735.4:c.*236C>A NP_079011.3:n.*236C>A
NM_024735.5:c.*236C>A MANE Select NP_079011.3:n.*236C>A
NM_001282683.2:c.*236C>A NP_001269612.1:n.*236C>A
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