Linked Data
dbSNP Id:
rs1808889107
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128853018_128853048del , CM000669.2:g.128853018_128853048del | GRCh38 |
| NC_000007.13:g.128493072_128493102del , CM000669.1:g.128493072_128493102del | GRCh37 |
| NC_000007.12:g.128280308_128280338del | NCBI36 |
| NG_011807.1:g.27590_27620del , LRG_870:g.27590_27620del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.6195_6208+17del (FLNC) | ||
| ENST00000325888.12:c.6195_6208+17del (FLNC) | ||
| ENST00000346177.6:c.6096_6109+17del (FLNC) | ||
| NM_001127487.1:c.6096_6109+17del (FLNC) | ||
| NM_001458.4:c.6195_6208+17del , LRG_870t1:c.6195_6208+17del (FLNC) | ||
| NR_149055.1:n.215+239_215+269del (FLNC-AS1) | ||
| NM_001127487.2:c.6096_6109+17del (FLNC) | ||
| NM_001458.5:c.6195_6208+17del (FLNC) |