Canonical Allele Identifier: CA578150172
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2936938
ClinVar RCV Id: RCV003791128
dbSNP Id: rs1242624751
gnomAD v2: 7-128481209-C-G
MyVariant Identifiers: chr7:g.128481209C>G (hg19) chr7:g.128841155C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841155C>G , CM000669.2:g.128841155C>G GRCh38
NC_000007.13:g.128481209C>G , CM000669.1:g.128481209C>G GRCh37
NC_000007.12:g.128268445C>G NCBI36
NG_011807.1:g.15727C>G , LRG_870:g.15727C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1814-15C>G MANE Select ENSP00000327145.8:n.1814-15C>G
ENST00000325888.12:c.1814-15C>G ENSP00000327145.8:n.1814-15C>G
ENST00000346177.6:c.1814-15C>G ENSP00000344002.6:n.1814-15C>G
NM_001127487.1:c.1814-15C>G NP_001120959.1:n.1814-15C>G
NM_001458.4:c.1814-15C>G , LRG_870t1:c.1814-15C>G NP_001449.3:n.1814-15C>G
NM_001127487.2:c.1814-15C>G NP_001120959.1:n.1814-15C>G
NM_001458.5:c.1814-15C>G MANE Select NP_001449.3:n.1814-15C>G
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