HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858339C= , CM000669.2:g.128858339C= | GRCh38 |
NC_000007.13:g.128498393C= , CM000669.1:g.128498393C= | GRCh37 |
NC_000007.12:g.128285629C= | NCBI36 |
NG_011807.1:g.32911C= , LRG_870:g.32911C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.7994C= (FLNC) MANE Select | ENSP00000327145.8:p.Thr2665= | |
ENST00000325888.12:c.7994C= (FLNC) | ENSP00000327145.8:p.Thr2665= | |
ENST00000346177.6:c.7895C= (FLNC) | ENSP00000344002.6:p.Thr2632= | |
NM_001127487.1:c.7895C= (FLNC) | NP_001120959.1:p.Thr2632= | |
NM_001458.4:c.7994C= , LRG_870t1:c.7994C= (FLNC) | NP_001449.3:p.Thr2665= | |
NR_149055.1:n.102+4186G= (FLNC-AS1) | ||
NM_001127487.2:c.7895C= (FLNC) | NP_001120959.1:p.Thr2632= | |
NM_001458.5:c.7994C= (FLNC) MANE Select | NP_001449.3:p.Thr2665= |