Linked Data
dbSNP Id:
rs764630195
ExAC:
7:128498591 C / T
gnomAD v2:
7-128498591-C-T
gnomAD v4:
7-128858537-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128858537C>T , CM000669.2:g.128858537C>T | GRCh38 |
| NC_000007.13:g.128498591C>T , CM000669.1:g.128498591C>T | GRCh37 |
| NC_000007.12:g.128285827C>T | NCBI36 |
| NG_011807.1:g.33109C>T , LRG_870:g.33109C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.*14C>T (FLNC) MANE Select | ENSP00000327145.8:n.*14C>T | |
| ENST00000325888.12:c.*14C>T (FLNC) | ENSP00000327145.8:n.*14C>T | |
| ENST00000346177.6:c.*14C>T (FLNC) | ENSP00000344002.6:n.*14C>T | |
| NM_001127487.1:c.*14C>T (FLNC) | NP_001120959.1:n.*14C>T | |
| NM_001458.4:c.*14C>T , LRG_870t1:c.*14C>T (FLNC) | NP_001449.3:n.*14C>T | |
| NR_149055.1:n.102+3988G>A (FLNC-AS1) | ||
| NM_001127487.2:c.*14C>T (FLNC) | NP_001120959.1:n.*14C>T | |
| NM_001458.5:c.*14C>T (FLNC) MANE Select | NP_001449.3:n.*14C>T |