Canonical Allele Identifier: CA16021079

Gene: FBXL4

Linked Data

• dbSNP Id: rs1299845150
• gnomAD v2: 6-99323567-C-T
• gnomAD v4: 6-98875691-C-T
• MyVariant Identifiers: chr6:g.99323567C>T (hg19) ; chr6:g.98875691C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875691C>T , CM000668.2:g.98875691C>T	GRCh38
NC_000006.11:g.99323567C>T , CM000668.1:g.99323567C>T	GRCh37
NC_000006.10:g.99430288C>T	NCBI36
NG_033903.1:g.77316G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1426G>A MANE Select	ENSP00000358247.1:p.Ala476Thr
ENST00000229971.2:c.1426G>A	ENSP00000229971.1:p.Ala476Thr
ENST00000369244.6:c.1426G>A	ENSP00000358247.1:p.Ala476Thr
NM_001278716.1:c.1426G>A	NP_001265645.1:p.Ala476Thr
NM_012160.4:c.1426G>A	NP_036292.2:p.Ala476Thr
NR_103836.1:n.1471G>A
XM_005266930.1:c.1354G>A	XP_005266987.1:p.Ala452Thr
XM_005266930.3:c.1354G>A	XP_005266987.1:p.Ala452Thr
XM_017010726.1:c.1426G>A	XP_016866215.1:p.Ala476Thr
XM_017010727.2:c.1354G>A	XP_016866216.1:p.Ala452Thr
XM_017010728.1:c.700G>A	XP_016866217.1:p.Ala234Thr
NM_001278716.2:c.1426G>A MANE Select	NP_001265645.1:p.Ala476Thr
NR_103836.2:n.1411G>A
NM_012160.5:c.1426G>A	NP_036292.2:p.Ala476Thr