Canonical Allele Identifier: CA830349915

Gene: FBXL4

Linked Data

• dbSNP Id: rs558316309
• gnomAD v3: 6-98875829-T-G
• gnomAD v4: 6-98875829-T-G
• MyVariant Identifiers: chr6:g.99323705T>G (hg19) ; chr6:g.98875829T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875829T>G , CM000668.2:g.98875829T>G	GRCh38
NC_000006.11:g.99323705T>G , CM000668.1:g.99323705T>G	GRCh37
NC_000006.10:g.99430426T>G	NCBI36
NG_033903.1:g.77178A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1390-102A>C MANE Select	ENSP00000358247.1:n.1390-102A>C
ENST00000229971.2:c.1390-102A>C	ENSP00000229971.1:n.1390-102A>C
ENST00000369244.6:c.1390-102A>C	ENSP00000358247.1:n.1390-102A>C
NM_001278716.1:c.1390-102A>C	NP_001265645.1:n.1390-102A>C
NM_012160.4:c.1390-102A>C	NP_036292.2:n.1390-102A>C
NR_103836.1:n.1435-102A>C
XM_005266930.1:c.1318-102A>C	XP_005266987.1:n.1318-102A>C
XM_005266930.3:c.1318-102A>C	XP_005266987.1:n.1318-102A>C
XM_017010726.1:c.1390-102A>C	XP_016866215.1:n.1390-102A>C
XM_017010727.2:c.1318-102A>C	XP_016866216.1:n.1318-102A>C
XM_017010728.1:c.664-102A>C	XP_016866217.1:n.664-102A>C
NM_001278716.2:c.1390-102A>C MANE Select	NP_001265645.1:n.1390-102A>C
NR_103836.2:n.1375-102A>C
NM_012160.5:c.1390-102A>C	NP_036292.2:n.1390-102A>C