HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858434A= , CM000669.2:g.128858434A= | GRCh38 |
NC_000007.13:g.128498488A= , CM000669.1:g.128498488A= | GRCh37 |
NC_000007.12:g.128285724A= | NCBI36 |
NG_011807.1:g.33006A= , LRG_870:g.33006A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.8089A= (FLNC) MANE Select | ENSP00000327145.8:p.Thr2697= | |
ENST00000325888.12:c.8089A= (FLNC) | ENSP00000327145.8:p.Thr2697= | |
ENST00000346177.6:c.7990A= (FLNC) | ENSP00000344002.6:p.Thr2664= | |
NM_001127487.1:c.7990A= (FLNC) | NP_001120959.1:p.Thr2664= | |
NM_001458.4:c.8089A= , LRG_870t1:c.8089A= (FLNC) | NP_001449.3:p.Thr2697= | |
NR_149055.1:n.102+4091T= (FLNC-AS1) | ||
NM_001127487.2:c.7990A= (FLNC) | NP_001120959.1:p.Thr2664= | |
NM_001458.5:c.8089A= (FLNC) MANE Select | NP_001449.3:p.Thr2697= |