Canonical Allele Identifier: CA3933416

Gene: FBXL4

Linked Data

• ClinVar Variation Id: 437777
• ClinVar RCV Id: RCV000502119 ; RCV001857197
• dbSNP Id: rs150523994
• ExAC: 6:99323399 G / C
• gnomAD v2: 6-99323399-G-C
• gnomAD v3: 6-98875523-G-C
• gnomAD v4: 6-98875523-G-C
• MyVariant Identifiers: chr6:g.99323399G>C (hg19) ; chr6:g.98875523G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875523G>C , CM000668.2:g.98875523G>C	GRCh38
NC_000006.11:g.99323399G>C , CM000668.1:g.99323399G>C	GRCh37
NC_000006.10:g.99430120G>C	NCBI36
NG_033903.1:g.77484C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1594C>G MANE Select	ENSP00000358247.1:p.Leu532Val
ENST00000229971.2:c.1594C>G	ENSP00000229971.1:p.Leu532Val
ENST00000369244.6:c.1594C>G	ENSP00000358247.1:p.Leu532Val
NM_001278716.1:c.1594C>G	NP_001265645.1:p.Leu532Val
NM_012160.4:c.1594C>G	NP_036292.2:p.Leu532Val
NR_103836.1:n.1639C>G
XM_005266930.1:c.1522C>G	XP_005266987.1:p.Leu508Val
XM_005266930.3:c.1522C>G	XP_005266987.1:p.Leu508Val
XM_017010726.1:c.1594C>G	XP_016866215.1:p.Leu532Val
XM_017010727.2:c.1522C>G	XP_016866216.1:p.Leu508Val
XM_017010728.1:c.868C>G	XP_016866217.1:p.Leu290Val
NM_001278716.2:c.1594C>G MANE Select	NP_001265645.1:p.Leu532Val
NR_103836.2:n.1579C>G
NM_012160.5:c.1594C>G	NP_036292.2:p.Leu532Val