Canonical Allele Identifier: CA369223716
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 471961
ClinVar RCV Id: RCV000532764
dbSNP Id: rs754733061
MyVariant Identifiers: chr7:g.128478379G>C (hg19) chr7:g.128838325G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128838325G>C , CM000669.2:g.128838325G>C GRCh38
NC_000007.13:g.128478379G>C , CM000669.1:g.128478379G>C GRCh37
NC_000007.12:g.128265615G>C NCBI36
NG_011807.1:g.12897G>C , LRG_870:g.12897G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.1106G>C MANE Select ENSP00000327145.8:p.Gly369Ala
ENST00000325888.12:c.1106G>C ENSP00000327145.8:p.Gly369Ala
ENST00000346177.6:c.1106G>C ENSP00000344002.6:p.Gly369Ala
NM_001127487.1:c.1106G>C NP_001120959.1:p.Gly369Ala
NM_001458.4:c.1106G>C , LRG_870t1:c.1106G>C NP_001449.3:p.Gly369Ala
NM_001127487.2:c.1106G>C NP_001120959.1:p.Gly369Ala
NM_001458.5:c.1106G>C MANE Select NP_001449.3:p.Gly369Ala
Search 100 bp 5'
Search 100 bp 3'