Canonical Allele Identifier: CA286122875

Gene: FBXO31

Linked Data

• dbSNP Id: rs533793773
• gnomAD v2: 16-87364658-G-A
• gnomAD v3: 16-87331052-G-A
• gnomAD v4: 16-87331052-G-A
• MyVariant Identifiers: chr16:g.87364658G>A (hg19) ; chr16:g.87331052G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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