Canonical Allele Identifier: CA369198145
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2574072
ClinVar RCV Id: RCV003492857
dbSNP Id: rs1392170803
MyVariant Identifiers: chr7:g.128485310G>C (hg19) chr7:g.128845256G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128845256G>C , CM000669.2:g.128845256G>C GRCh38
NC_000007.13:g.128485310G>C , CM000669.1:g.128485310G>C GRCh37
NC_000007.12:g.128272546G>C NCBI36
NG_011807.1:g.19828G>C , LRG_870:g.19828G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3790+1G>C MANE Select ENSP00000327145.8:n.3790+1G>C
ENST00000325888.12:c.3790+1G>C ENSP00000327145.8:n.3790+1G>C
ENST00000346177.6:c.3790+1G>C ENSP00000344002.6:n.3790+1G>C
NM_001127487.1:c.3790+1G>C NP_001120959.1:n.3790+1G>C
NM_001458.4:c.3790+1G>C , LRG_870t1:c.3790+1G>C NP_001449.3:n.3790+1G>C
NM_001127487.2:c.3790+1G>C NP_001120959.1:n.3790+1G>C
NM_001458.5:c.3790+1G>C MANE Select NP_001449.3:n.3790+1G>C
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