Canonical Allele Identifier: CA4475379
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 934479
ClinVar RCV Id: RCV001202879 RCV002339506 RCV003145372
dbSNP Id: rs374729872
ExAC: 7:128488119 G / A
gnomAD v2: 7-128488119-G-A
gnomAD v3: 7-128848065-G-A
gnomAD v4: 7-128848065-G-A
MyVariant Identifiers: chr7:g.128488119G>A (hg19) chr7:g.128848065G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128848065G>A , CM000669.2:g.128848065G>A GRCh38
NC_000007.13:g.128488119G>A , CM000669.1:g.128488119G>A GRCh37
NC_000007.12:g.128275355G>A NCBI36
NG_011807.1:g.22637G>A , LRG_870:g.22637G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.4577G>A MANE Select ENSP00000327145.8:p.Arg1526His
ENST00000325888.12:c.4577G>A ENSP00000327145.8:p.Arg1526His
ENST00000346177.6:c.4577G>A ENSP00000344002.6:p.Arg1526His
NM_001127487.1:c.4577G>A NP_001120959.1:p.Arg1526His
NM_001458.4:c.4577G>A , LRG_870t1:c.4577G>A NP_001449.3:p.Arg1526His
NM_001127487.2:c.4577G>A NP_001120959.1:p.Arg1526His
NM_001458.5:c.4577G>A MANE Select NP_001449.3:p.Arg1526His
Search 100 bp 5'
Search 100 bp 3'