Canonical Allele Identifier: CA569080358

Gene: FBXL4

Linked Data

• dbSNP Id: rs1293440464
• gnomAD v2: 6-99322147-T-A
• gnomAD v4: 6-98874271-T-A
• MyVariant Identifiers: chr6:g.99322147T>A (hg19) ; chr6:g.98874271T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98874271T>A , CM000668.2:g.98874271T>A	GRCh38
NC_000006.11:g.99322147T>A , CM000668.1:g.99322147T>A	GRCh37
NC_000006.10:g.99428868T>A	NCBI36
NG_033903.1:g.78736A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.*7A>T MANE Select	ENSP00000358247.1:n.*7A>T
ENST00000229971.2:c.*7A>T	ENSP00000229971.1:n.*7A>T
ENST00000369244.6:c.*7A>T	ENSP00000358247.1:n.*7A>T
NM_001278716.1:c.*7A>T	NP_001265645.1:n.*7A>T
NM_012160.4:c.*7A>T	NP_036292.2:n.*7A>T
NR_103836.1:n.1918A>T
XM_005266930.1:c.*7A>T	XP_005266987.1:n.*7A>T
XM_005266930.3:c.*7A>T	XP_005266987.1:n.*7A>T
XM_017010726.1:c.*7A>T	XP_016866215.1:n.*7A>T
XM_017010727.2:c.*7A>T	XP_016866216.1:n.*7A>T
XM_017010728.1:c.*7A>T	XP_016866217.1:n.*7A>T
NM_001278716.2:c.*7A>T MANE Select	NP_001265645.1:n.*7A>T
NR_103836.2:n.1858A>T
NM_012160.5:c.*7A>T	NP_036292.2:n.*7A>T