Canonical Allele Identifier: CA4474851
Gene: FLNC HGNC NCBI

Linked Data

dbSNP Id: rs779309552
ExAC: 7:128483658 G / A
gnomAD v2: 7-128483658-G-A
gnomAD v3: 7-128843604-G-A
gnomAD v4: 7-128843604-G-A
MyVariant Identifiers: chr7:g.128483658G>A (hg19) chr7:g.128843604G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128843604G>A , CM000669.2:g.128843604G>A GRCh38
NC_000007.13:g.128483658G>A , CM000669.1:g.128483658G>A GRCh37
NC_000007.12:g.128270894G>A NCBI36
NG_011807.1:g.18176G>A , LRG_870:g.18176G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325888.13:c.2811+27G>A MANE Select ENSP00000327145.8:n.2811+27G>A
ENST00000325888.12:c.2811+27G>A ENSP00000327145.8:n.2811+27G>A
ENST00000346177.6:c.2811+27G>A ENSP00000344002.6:n.2811+27G>A
NM_001127487.1:c.2811+27G>A NP_001120959.1:n.2811+27G>A
NM_001458.4:c.2811+27G>A , LRG_870t1:c.2811+27G>A NP_001449.3:n.2811+27G>A
NM_001127487.2:c.2811+27G>A NP_001120959.1:n.2811+27G>A
NM_001458.5:c.2811+27G>A MANE Select NP_001449.3:n.2811+27G>A
Search 100 bp 5'
Search 100 bp 3'