Canonical Allele Identifier: CA369196729
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1378505
ClinVar RCV Id: RCV001914630
dbSNP Id: rs2128936421
MyVariant Identifiers: chr7:g.128484914A>G (hg19) chr7:g.128844860A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128844860A>G , CM000669.2:g.128844860A>G GRCh38
NC_000007.13:g.128484914A>G , CM000669.1:g.128484914A>G GRCh37
NC_000007.12:g.128272150A>G NCBI36
NG_011807.1:g.19432A>G , LRG_870:g.19432A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.3395A>G MANE Select ENSP00000327145.8:p.Asn1132Ser
ENST00000325888.12:c.3395A>G ENSP00000327145.8:p.Asn1132Ser
ENST00000346177.6:c.3395A>G ENSP00000344002.6:p.Asn1132Ser
NM_001127487.1:c.3395A>G NP_001120959.1:p.Asn1132Ser
NM_001458.4:c.3395A>G , LRG_870t1:c.3395A>G NP_001449.3:p.Asn1132Ser
NM_001127487.2:c.3395A>G NP_001120959.1:p.Asn1132Ser
NM_001458.5:c.3395A>G MANE Select NP_001449.3:p.Asn1132Ser
Search 100 bp 5'
Search 100 bp 3'