Linked Data
ClinVar Variation Id:
472150
dbSNP Id:
rs375259002
ExAC:
7:128494627 C / T
gnomAD v2:
7-128494627-C-T
gnomAD v3:
7-128854573-C-T
gnomAD v4:
7-128854573-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128854573C>T , CM000669.2:g.128854573C>T | GRCh38 |
| NC_000007.13:g.128494627C>T , CM000669.1:g.128494627C>T | GRCh37 |
| NC_000007.12:g.128281863C>T | NCBI36 |
| NG_011807.1:g.29145C>T , LRG_870:g.29145C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000325888.13:c.6888C>T (FLNC) MANE Select | ENSP00000327145.8:p.His2296= | |
| ENST00000325888.12:c.6888C>T (FLNC) | ENSP00000327145.8:p.His2296= | |
| ENST00000346177.6:c.6789C>T (FLNC) | ENSP00000344002.6:p.His2263= | |
| NM_001127487.1:c.6789C>T (FLNC) | NP_001120959.1:p.His2263= | |
| NM_001458.4:c.6888C>T , LRG_870t1:c.6888C>T (FLNC) | NP_001449.3:p.His2296= | |
| NR_149055.1:n.103-1176G>A (FLNC-AS1) | ||
| NM_001127487.2:c.6789C>T (FLNC) | NP_001120959.1:p.His2263= | |
| NM_001458.5:c.6888C>T (FLNC) MANE Select | NP_001449.3:p.His2296= |