Canonical Allele Identifier: CA569080393

Gene: FBXL4

Linked Data

• dbSNP Id: rs1432858901
• gnomAD v2: 6-99323177-G-C
• gnomAD v3: 6-98875301-G-C
• gnomAD v4: 6-98875301-G-C
• MyVariant Identifiers: chr6:g.99323177G>C (hg19) ; chr6:g.98875301G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875301G>C , CM000668.2:g.98875301G>C	GRCh38
NC_000006.11:g.99323177G>C , CM000668.1:g.99323177G>C	GRCh37
NC_000006.10:g.99429898G>C	NCBI36
NG_033903.1:g.77706C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+114C>G MANE Select	ENSP00000358247.1:n.1702+114C>G
ENST00000229971.2:c.1702+114C>G	ENSP00000229971.1:n.1702+114C>G
ENST00000369244.6:c.1702+114C>G	ENSP00000358247.1:n.1702+114C>G
NM_001278716.1:c.1702+114C>G	NP_001265645.1:n.1702+114C>G
NM_012160.4:c.1702+114C>G	NP_036292.2:n.1702+114C>G
NR_103836.1:n.1747+114C>G
XM_005266930.1:c.1630+114C>G	XP_005266987.1:n.1630+114C>G
XM_005266930.3:c.1630+114C>G	XP_005266987.1:n.1630+114C>G
XM_017010726.1:c.1702+114C>G	XP_016866215.1:n.1702+114C>G
XM_017010727.2:c.1630+114C>G	XP_016866216.1:n.1630+114C>G
XM_017010728.1:c.976+114C>G	XP_016866217.1:n.976+114C>G
NM_001278716.2:c.1702+114C>G MANE Select	NP_001265645.1:n.1702+114C>G
NR_103836.2:n.1687+114C>G
NM_012160.5:c.1702+114C>G	NP_036292.2:n.1702+114C>G