Canonical Allele Identifier: CA4474507
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1046144
ClinVar RCV Id: RCV001350661
dbSNP Id: rs779240577
ExAC: 7:128481232 A / G
gnomAD v2: 7-128481232-A-G
gnomAD v3: 7-128841178-A-G
gnomAD v4: 7-128841178-A-G
MyVariant Identifiers: chr7:g.128481232A>G (hg19) chr7:g.128841178A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128841178A>G , CM000669.2:g.128841178A>G GRCh38
NC_000007.13:g.128481232A>G , CM000669.1:g.128481232A>G GRCh37
NC_000007.12:g.128268468A>G NCBI36
NG_011807.1:g.15750A>G , LRG_870:g.15750A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.1822A>G MANE Select ENSP00000327145.8:p.Ile608Val
ENST00000325888.12:c.1822A>G ENSP00000327145.8:p.Ile608Val
ENST00000346177.6:c.1822A>G ENSP00000344002.6:p.Ile608Val
NM_001127487.1:c.1822A>G NP_001120959.1:p.Ile608Val
NM_001458.4:c.1822A>G , LRG_870t1:c.1822A>G NP_001449.3:p.Ile608Val
NM_001127487.2:c.1822A>G NP_001120959.1:p.Ile608Val
NM_001458.5:c.1822A>G MANE Select NP_001449.3:p.Ile608Val
Search 100 bp 5'
Search 100 bp 3'