Canonical Allele Identifier: CA166185256
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1667008
ClinVar RCV Id: RCV002186599
dbSNP Id: rs746914067
gnomAD v2: 7-128489378-A-G
gnomAD v4: 7-128849324-A-G
MyVariant Identifiers: chr7:g.128489378A>G (hg19) chr7:g.128849324A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849324A>G , CM000669.2:g.128849324A>G GRCh38
NC_000007.13:g.128489378A>G , CM000669.1:g.128489378A>G GRCh37
NC_000007.12:g.128276614A>G NCBI36
NG_011807.1:g.23896A>G , LRG_870:g.23896A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.4952-7A>G MANE Select ENSP00000327145.8:n.4952-7A>G
ENST00000325888.12:c.4952-7A>G ENSP00000327145.8:n.4952-7A>G
ENST00000346177.6:c.4952-7A>G ENSP00000344002.6:n.4952-7A>G
NM_001127487.1:c.4952-7A>G NP_001120959.1:n.4952-7A>G
NM_001458.4:c.4952-7A>G , LRG_870t1:c.4952-7A>G NP_001449.3:n.4952-7A>G
NM_001127487.2:c.4952-7A>G NP_001120959.1:n.4952-7A>G
NM_001458.5:c.4952-7A>G MANE Select NP_001449.3:n.4952-7A>G
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Search 100 bp 3'