Canonical Allele Identifier: CA624112778

Gene: FBXO31

Linked Data

• dbSNP Id: rs1214919295
• gnomAD v2: 16-87364653-G-C
• gnomAD v3: 16-87331047-G-C
• gnomAD v4: 16-87331047-G-C
• MyVariant Identifiers: chr16:g.87364653G>C (hg19) ; chr16:g.87331047G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.87331047G>C , CM000678.2:g.87331047G>C	GRCh38
NC_000016.9:g.87364653G>C , CM000678.1:g.87364653G>C	GRCh37
NC_000016.8:g.85922154G>C	NCBI36
NG_047196.1:g.66061C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000636077.2:c.*241C>G	ENSP00000490402.2:n.*241C>G
ENST00000311635.12:c.*241C>G MANE Select	ENSP00000310841.4:n.*241C>G
ENST00000618298.6:c.*241C>G	ENSP00000479703.1:n.*241C>G
ENST00000311635.11:c.*241C>G	ENSP00000310841.4:n.*241C>G
ENST00000565593.1:c.*567C>G	ENSP00000455772.1:n.*567C>G
ENST00000568879.1:c.388+2839C>G
ENST00000618298.4:c.*241C>G	ENSP00000479703.1:n.*241C>G
NM_001282683.1:c.*241C>G	NP_001269612.1:n.*241C>G
NM_024735.4:c.*241C>G	NP_079011.3:n.*241C>G
NM_024735.5:c.*241C>G MANE Select	NP_079011.3:n.*241C>G
NM_001282683.2:c.*241C>G	NP_001269612.1:n.*241C>G