Canonical Allele Identifier: CA143895286

Gene: FBXL4

Linked Data

• ClinVar Variation Id: 1181505
• ClinVar RCV Id: RCV001538908
• dbSNP Id: rs111226417
• gnomAD v2: 6-99322064-C-G
• gnomAD v3: 6-98874188-C-G
• gnomAD v4: 6-98874188-C-G
• MyVariant Identifiers: chr6:g.99322064C>G (hg19) ; chr6:g.98874188C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874188C>G , CM000668.2:g.98874188C>G	GRCh38
NC_000006.11:g.99322064C>G , CM000668.1:g.99322064C>G	GRCh37
NC_000006.10:g.99428785C>G	NCBI36
NG_033903.1:g.78819G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*90G>C MANE Select	ENSP00000358247.1:n.*90G>C
ENST00000229971.2:c.*90G>C	ENSP00000229971.1:n.*90G>C
ENST00000369244.6:c.*90G>C	ENSP00000358247.1:n.*90G>C
NM_001278716.1:c.*90G>C	NP_001265645.1:n.*90G>C
NM_012160.4:c.*90G>C	NP_036292.2:n.*90G>C
NR_103836.1:n.2001G>C
XM_005266930.1:c.*90G>C	XP_005266987.1:n.*90G>C
XM_005266930.3:c.*90G>C	XP_005266987.1:n.*90G>C
XM_017010726.1:c.*90G>C	XP_016866215.1:n.*90G>C
XM_017010727.2:c.*90G>C	XP_016866216.1:n.*90G>C
XM_017010728.1:c.*90G>C	XP_016866217.1:n.*90G>C
NM_001278716.2:c.*90G>C MANE Select	NP_001265645.1:n.*90G>C
NR_103836.2:n.1941G>C
NM_012160.5:c.*90G>C	NP_036292.2:n.*90G>C