Canonical Allele Identifier: CA365091345

Gene: FBXL4

Linked Data

• dbSNP Id: rs1382436369
• gnomAD v2: 6-99374714-C-T
• gnomAD v4: 6-98926838-C-T
• MyVariant Identifiers: chr6:g.99374714C>T (hg19) ; chr6:g.98926838C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926838C>T , CM000668.2:g.98926838C>T	GRCh38
NC_000006.11:g.99374714C>T , CM000668.1:g.99374714C>T	GRCh37
NC_000006.10:g.99481435C>T	NCBI36
NG_033903.1:g.26169G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369244.7:c.151G>A MANE Select	ENSP00000358247.1:p.Val51Ile
ENST00000229971.2:c.151G>A	ENSP00000229971.1:p.Val51Ile
ENST00000369244.6:c.151G>A	ENSP00000358247.1:p.Val51Ile
NM_001278716.1:c.151G>A	NP_001265645.1:p.Val51Ile
NM_012160.4:c.151G>A	NP_036292.2:p.Val51Ile
NR_103836.1:n.542G>A
NR_103837.1:n.542G>A
XM_005266930.1:c.151G>A	XP_005266987.1:p.Val51Ile
XM_011535748.1:c.151G>A	XP_011534050.1:p.Val51Ile
XM_005266930.3:c.151G>A	XP_005266987.1:p.Val51Ile
XM_011535748.3:c.151G>A	XP_011534050.1:p.Val51Ile
XM_017010726.1:c.151G>A	XP_016866215.1:p.Val51Ile
XM_017010727.2:c.151G>A	XP_016866216.1:p.Val51Ile
XM_017010728.1:c.-652G>A	XP_016866217.1:n.-652G>A
NM_001278716.2:c.151G>A MANE Select	NP_001265645.1:p.Val51Ile
NR_103836.2:n.482G>A
NR_103837.2:n.482G>A
NM_012160.5:c.151G>A	NP_036292.2:p.Val51Ile