Canonical Allele Identifier: CA166212767
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1619650
ClinVar RCV Id: RCV002089007 RCV003426336
dbSNP Id: rs867399299
gnomAD v2: 7-128475387-G-A
gnomAD v3: 7-128835333-G-A
gnomAD v4: 7-128835333-G-A
MyVariant Identifiers: chr7:g.128475387G>A (hg19) chr7:g.128835333G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128835333G>A , CM000669.2:g.128835333G>A GRCh38
NC_000007.13:g.128475387G>A , CM000669.1:g.128475387G>A GRCh37
NC_000007.12:g.128262623G>A NCBI36
NG_011807.1:g.9905G>A , LRG_870:g.9905G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.360G>A MANE Select ENSP00000327145.8:p.Lys120=
ENST00000325888.12:c.360G>A ENSP00000327145.8:p.Lys120=
ENST00000346177.6:c.360G>A ENSP00000344002.6:p.Lys120=
NM_001127487.1:c.360G>A NP_001120959.1:p.Lys120=
NM_001458.4:c.360G>A , LRG_870t1:c.360G>A NP_001449.3:p.Lys120=
NM_001127487.2:c.360G>A NP_001120959.1:p.Lys120=
NM_001458.5:c.360G>A MANE Select NP_001449.3:p.Lys120=
Search 100 bp 5'
Search 100 bp 3'