Canonical Allele Identifier: CA341859
Gene: FLNB HGNC NCBI

Linked Data

ClinVar Variation Id: 21292
ClinVar RCV Id: RCV000020455
dbSNP Id: rs80356516
MyVariant Identifiers: chr3:g.58131722G>A (hg19) chr3:g.58145995G>A (hg38)
PubMed: PMID:16648377 PMID:16801345 PMID:20301736
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.58145995G>A , CM000665.2:g.58145995G>A GRCh38
NC_000003.11:g.58131722G>A , CM000665.1:g.58131722G>A GRCh37
NC_000003.10:g.58106762G>A NCBI36
NG_012801.1:g.142596G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682297.1:n.852G>A
ENST00000682871.1:c.5380G>A ENSP00000507805.1:p.Gly1794Arg
ENST00000683925.1:n.1598G>A
ENST00000684439.1:n.1811G>A
ENST00000684506.1:c.*4053G>A ENSP00000507728.1:n.*4053G>A
ENST00000684607.1:c.5521G>A ENSP00000508224.1:p.Gly1841Arg
ENST00000295956.9:c.5500G>A MANE Select ENSP00000295956.5:p.Gly1834Arg
ENST00000295956.8:c.5500G>A ENSP00000295956.4:p.Gly1834Arg
ENST00000358537.7:c.5428G>A ENSP00000351339.3:p.Gly1810Arg
ENST00000429972.6:c.5467G>A ENSP00000415599.2:p.Gly1823Arg
ENST00000481470.5:n.1768G>A
ENST00000490882.5:c.5593G>A ENSP00000420213.1:p.Gly1865Arg
ENST00000493452.5:c.4921G>A ENSP00000418510.1:p.Gly1641Arg
NM_001164317.1:c.5593G>A NP_001157789.1:p.Gly1865Arg
NM_001164318.1:c.5467G>A NP_001157790.1:p.Gly1823Arg
NM_001164319.1:c.5428G>A NP_001157791.1:p.Gly1810Arg
NM_001457.3:c.5500G>A NP_001448.2:p.Gly1834Arg
XM_005264977.1:c.5560G>A XP_005265034.1:p.Gly1854Arg
XM_005264978.1:c.5521G>A XP_005265035.1:p.Gly1841Arg
XM_005264981.1:c.5593G>A XP_005265038.1:p.Gly1865Arg
XR_940396.1:n.5738G>A
XM_005264978.2:c.5521G>A XP_005265035.1:p.Gly1841Arg
XR_001740065.1:n.5738G>A
XR_940396.2:n.5738G>A
NM_001164317.2:c.5593G>A NP_001157789.1:p.Gly1865Arg
NM_001164318.2:c.5467G>A NP_001157790.1:p.Gly1823Arg
NM_001164319.2:c.5428G>A NP_001157791.1:p.Gly1810Arg
NM_001457.4:c.5500G>A MANE Select NP_001448.2:p.Gly1834Arg
Search 100 bp 5'
Search 100 bp 3'