Canonical Allele Identifier: CA2468846

Gene: FLNB

Linked Data

• ClinVar Variation Id: 389236
• ClinVar RCV Id: RCV000419106 ; RCV002522498
• dbSNP Id: rs72884428
• ExAC: 3:58121695 A / G
• gnomAD v2: 3-58121695-A-G
• gnomAD v3: 3-58135968-A-G
• gnomAD v4: 3-58135968-A-G
• MyVariant Identifiers: chr3:g.58121695A>G (hg19) ; chr3:g.58135968A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58135968A>G , CM000665.2:g.58135968A>G	GRCh38
NC_000003.11:g.58121695A>G , CM000665.1:g.58121695A>G	GRCh37
NC_000003.10:g.58096735A>G	NCBI36
NG_012801.1:g.132569A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682297.1:n.96-11A>G
ENST00000682868.1:n.6714-11A>G
ENST00000682871.1:c.4765-11A>G	ENSP00000507805.1:n.4765-11A>G
ENST00000684506.1:c.*3297-11A>G	ENSP00000507728.1:n.*3297-11A>G
ENST00000684607.1:c.4765-11A>G	ENSP00000508224.1:n.4765-11A>G
ENST00000295956.9:c.4672-11A>G MANE Select	ENSP00000295956.5:n.4672-11A>G
ENST00000295956.8:c.4672-11A>G	ENSP00000295956.4:n.4672-11A>G
ENST00000358537.7:c.4672-11A>G	ENSP00000351339.3:n.4672-11A>G
ENST00000429972.6:c.4672-11A>G	ENSP00000415599.2:n.4672-11A>G
ENST00000481470.5:n.1012-11A>G
ENST00000490882.5:c.4765-11A>G	ENSP00000420213.1:n.4765-11A>G
ENST00000493452.5:c.4165-11A>G	ENSP00000418510.1:n.4165-11A>G
NM_001164317.1:c.4765-11A>G	NP_001157789.1:n.4765-11A>G
NM_001164318.1:c.4672-11A>G	NP_001157790.1:n.4672-11A>G
NM_001164319.1:c.4672-11A>G	NP_001157791.1:n.4672-11A>G
NM_001457.3:c.4672-11A>G	NP_001448.2:n.4672-11A>G
XM_005264977.1:c.4765-11A>G	XP_005265034.1:n.4765-11A>G
XM_005264978.1:c.4765-11A>G	XP_005265035.1:n.4765-11A>G
XM_005264981.1:c.4765-11A>G	XP_005265038.1:n.4765-11A>G
XR_940396.1:n.4910-11A>G
XM_005264978.2:c.4765-11A>G	XP_005265035.1:n.4765-11A>G
XR_001740065.1:n.4910-11A>G
XR_940396.2:n.4910-11A>G
NM_001164317.2:c.4765-11A>G	NP_001157789.1:n.4765-11A>G
NM_001164318.2:c.4672-11A>G	NP_001157790.1:n.4672-11A>G
NM_001164319.2:c.4672-11A>G	NP_001157791.1:n.4672-11A>G
NM_001457.4:c.4672-11A>G MANE Select	NP_001448.2:n.4672-11A>G