Canonical Allele Identifier: CA2469068

Gene: FLNB

Linked Data

• ClinVar Variation Id: 3016882
• ClinVar RCV Id: RCV003879017
• dbSNP Id: rs373474943
• ExAC: 3:58131631 G / A
• gnomAD v2: 3-58131631-G-A
• gnomAD v3: 3-58145904-G-A
• gnomAD v4: 3-58145904-G-A
• MyVariant Identifiers: chr3:g.58131631G>A (hg19) ; chr3:g.58145904G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58145904G>A , CM000665.2:g.58145904G>A	GRCh38
NC_000003.11:g.58131631G>A , CM000665.1:g.58131631G>A	GRCh37
NC_000003.10:g.58106671G>A	NCBI36
NG_012801.1:g.142505G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682297.1:n.778-17G>A
ENST00000682871.1:c.5306-17G>A	ENSP00000507805.1:n.5306-17G>A
ENST00000683925.1:n.1507G>A
ENST00000684439.1:n.1737-17G>A
ENST00000684506.1:c.*3979-17G>A	ENSP00000507728.1:n.*3979-17G>A
ENST00000684607.1:c.5447-17G>A	ENSP00000508224.1:n.5447-17G>A
ENST00000295956.9:c.5426-17G>A MANE Select	ENSP00000295956.5:n.5426-17G>A
ENST00000295956.8:c.5426-17G>A	ENSP00000295956.4:n.5426-17G>A
ENST00000358537.7:c.5354-17G>A	ENSP00000351339.3:n.5354-17G>A
ENST00000429972.6:c.5393-17G>A	ENSP00000415599.2:n.5393-17G>A
ENST00000481470.5:n.1694-17G>A
ENST00000490882.5:c.5519-17G>A	ENSP00000420213.1:n.5519-17G>A
ENST00000493452.5:c.4847-17G>A	ENSP00000418510.1:n.4847-17G>A
NM_001164317.1:c.5519-17G>A	NP_001157789.1:n.5519-17G>A
NM_001164318.1:c.5393-17G>A	NP_001157790.1:n.5393-17G>A
NM_001164319.1:c.5354-17G>A	NP_001157791.1:n.5354-17G>A
NM_001457.3:c.5426-17G>A	NP_001448.2:n.5426-17G>A
XM_005264977.1:c.5486-17G>A	XP_005265034.1:n.5486-17G>A
XM_005264978.1:c.5447-17G>A	XP_005265035.1:n.5447-17G>A
XM_005264981.1:c.5519-17G>A	XP_005265038.1:n.5519-17G>A
XR_940396.1:n.5664-17G>A
XM_005264978.2:c.5447-17G>A	XP_005265035.1:n.5447-17G>A
XR_001740065.1:n.5664-17G>A
XR_940396.2:n.5664-17G>A
NM_001164317.2:c.5519-17G>A	NP_001157789.1:n.5519-17G>A
NM_001164318.2:c.5393-17G>A	NP_001157790.1:n.5393-17G>A
NM_001164319.2:c.5354-17G>A	NP_001157791.1:n.5354-17G>A
NM_001457.4:c.5426-17G>A MANE Select	NP_001448.2:n.5426-17G>A