Canonical Allele Identifier: CA343268
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 38960
ClinVar RCV Id: RCV004528148
dbSNP Id: rs80356505

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58136142G>A , CM000665.2:g.58136142G>A GRCh38
NC_000003.11:g.58121869G>A , CM000665.1:g.58121869G>A GRCh37
NC_000003.10:g.58096909G>A NCBI36
NG_012801.1:g.132743G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682297.1:n.259G>A
ENST00000682868.1:n.6877G>A
ENST00000682871.1:c.4928G>A ENSP00000507805.1:p.Gly1643Asp
ENST00000684506.1:c.*3460G>A ENSP00000507728.1:n.*3460G>A
ENST00000684607.1:c.4928G>A ENSP00000508224.1:p.Gly1643Asp
ENST00000295956.9:c.4835G>A MANE Select ENSP00000295956.5:p.Gly1612Asp
ENST00000295956.8:c.4835G>A ENSP00000295956.4:p.Gly1612Asp
ENST00000358537.7:c.4835G>A ENSP00000351339.3:p.Gly1612Asp
ENST00000429972.6:c.4835G>A ENSP00000415599.2:p.Gly1612Asp
ENST00000481470.5:n.1175G>A
ENST00000490882.5:c.4928G>A ENSP00000420213.1:p.Gly1643Asp
ENST00000493452.5:c.4328G>A ENSP00000418510.1:p.Gly1443Asp
NM_001164317.1:c.4928G>A NP_001157789.1:p.Gly1643Asp
NM_001164318.1:c.4835G>A NP_001157790.1:p.Gly1612Asp
NM_001164319.1:c.4835G>A NP_001157791.1:p.Gly1612Asp
NM_001457.3:c.4835G>A NP_001448.2:p.Gly1612Asp
XM_005264977.1:c.4928G>A XP_005265034.1:p.Gly1643Asp
XM_005264978.1:c.4928G>A XP_005265035.1:p.Gly1643Asp
XM_005264981.1:c.4928G>A XP_005265038.1:p.Gly1643Asp
XR_940396.1:n.5073G>A
XM_005264978.2:c.4928G>A XP_005265035.1:p.Gly1643Asp
XR_001740065.1:n.5073G>A
XR_940396.2:n.5073G>A
NM_001164317.2:c.4928G>A NP_001157789.1:p.Gly1643Asp
NM_001164318.2:c.4835G>A NP_001157790.1:p.Gly1612Asp
NM_001164319.2:c.4835G>A NP_001157791.1:p.Gly1612Asp
NM_001457.4:c.4835G>A MANE Select NP_001448.2:p.Gly1612Asp