HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858617C>T , CM000669.2:g.128858617C>T | GRCh38 |
NC_000007.13:g.128498671C>T , CM000669.1:g.128498671C>T | GRCh37 |
NC_000007.12:g.128285907C>T | NCBI36 |
NG_011807.1:g.33189C>T , LRG_870:g.33189C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.*94C>T (FLNC) MANE Select | ENSP00000327145.8:n.*94C>T | |
ENST00000325888.12:c.*94C>T (FLNC) | ENSP00000327145.8:n.*94C>T | |
ENST00000346177.6:c.*94C>T (FLNC) | ENSP00000344002.6:n.*94C>T | |
NM_001127487.1:c.*94C>T (FLNC) | NP_001120959.1:n.*94C>T | |
NM_001458.4:c.*94C>T , LRG_870t1:c.*94C>T (FLNC) | NP_001449.3:n.*94C>T | |
NR_149055.1:n.102+3908G>A (FLNC-AS1) | ||
NM_001127487.2:c.*94C>T (FLNC) | NP_001120959.1:n.*94C>T | |
NM_001458.5:c.*94C>T (FLNC) MANE Select | NP_001449.3:n.*94C>T |