Canonical Allele Identifier: CA2468871

Gene: FLNB

Linked Data

• ClinVar Variation Id: 1090692
• ClinVar RCV Id: RCV001409926
• dbSNP Id: rs774105587
• ExAC: 3:58121854 G / A
• gnomAD v2: 3-58121854-G-A
• gnomAD v3: 3-58136127-G-A
• gnomAD v4: 3-58136127-G-A
• MyVariant Identifiers: chr3:g.58121854G>A (hg19) ; chr3:g.58136127G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58136127G>A , CM000665.2:g.58136127G>A	GRCh38
NC_000003.11:g.58121854G>A , CM000665.1:g.58121854G>A	GRCh37
NC_000003.10:g.58096894G>A	NCBI36
NG_012801.1:g.132728G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682297.1:n.244G>A
ENST00000682868.1:n.6862G>A
ENST00000682871.1:c.4913G>A	ENSP00000507805.1:p.Arg1638Gln
ENST00000684506.1:c.*3445G>A	ENSP00000507728.1:n.*3445G>A
ENST00000684607.1:c.4913G>A	ENSP00000508224.1:p.Arg1638Gln
ENST00000295956.9:c.4820G>A MANE Select	ENSP00000295956.5:p.Arg1607Gln
ENST00000295956.8:c.4820G>A	ENSP00000295956.4:p.Arg1607Gln
ENST00000358537.7:c.4820G>A	ENSP00000351339.3:p.Arg1607Gln
ENST00000429972.6:c.4820G>A	ENSP00000415599.2:p.Arg1607Gln
ENST00000481470.5:n.1160G>A
ENST00000490882.5:c.4913G>A	ENSP00000420213.1:p.Arg1638Gln
ENST00000493452.5:c.4313G>A	ENSP00000418510.1:p.Arg1438Gln
NM_001164317.1:c.4913G>A	NP_001157789.1:p.Arg1638Gln
NM_001164318.1:c.4820G>A	NP_001157790.1:p.Arg1607Gln
NM_001164319.1:c.4820G>A	NP_001157791.1:p.Arg1607Gln
NM_001457.3:c.4820G>A	NP_001448.2:p.Arg1607Gln
XM_005264977.1:c.4913G>A	XP_005265034.1:p.Arg1638Gln
XM_005264978.1:c.4913G>A	XP_005265035.1:p.Arg1638Gln
XM_005264981.1:c.4913G>A	XP_005265038.1:p.Arg1638Gln
XR_940396.1:n.5058G>A
XM_005264978.2:c.4913G>A	XP_005265035.1:p.Arg1638Gln
XR_001740065.1:n.5058G>A
XR_940396.2:n.5058G>A
NM_001164317.2:c.4913G>A	NP_001157789.1:p.Arg1638Gln
NM_001164318.2:c.4820G>A	NP_001157790.1:p.Arg1607Gln
NM_001164319.2:c.4820G>A	NP_001157791.1:p.Arg1607Gln
NM_001457.4:c.4820G>A MANE Select	NP_001448.2:p.Arg1607Gln