Canonical Allele Identifier: CA2634762476
Gene: FBXO31 HGNC NCBI

Linked Data

gnomAD v4: 16-87331050-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.87331050T>G , CM000678.2:g.87331050T>G GRCh38
NC_000016.9:g.87364656T>G , CM000678.1:g.87364656T>G GRCh37
NC_000016.8:g.85922157T>G NCBI36
NG_047196.1:g.66058A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000636077.2:c.*238A>C ENSP00000490402.2:n.*238A>C
ENST00000311635.12:c.*238A>C MANE Select ENSP00000310841.4:n.*238A>C
ENST00000618298.6:c.*238A>C ENSP00000479703.1:n.*238A>C
ENST00000311635.11:c.*238A>C ENSP00000310841.4:n.*238A>C
ENST00000565593.1:c.*564A>C ENSP00000455772.1:n.*564A>C
ENST00000568879.1:c.388+2836A>C
ENST00000618298.4:c.*238A>C ENSP00000479703.1:n.*238A>C
NM_001282683.1:c.*238A>C NP_001269612.1:n.*238A>C
NM_024735.4:c.*238A>C NP_079011.3:n.*238A>C
NM_024735.5:c.*238A>C MANE Select NP_079011.3:n.*238A>C
NM_001282683.2:c.*238A>C NP_001269612.1:n.*238A>C
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