HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858436T>C , CM000669.2:g.128858436T>C | GRCh38 |
NC_000007.13:g.128498490T>C , CM000669.1:g.128498490T>C | GRCh37 |
NC_000007.12:g.128285726T>C | NCBI36 |
NG_011807.1:g.33008T>C , LRG_870:g.33008T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.8091T>C (FLNC) MANE Select | ENSP00000327145.8:p.Thr2697= | |
ENST00000325888.12:c.8091T>C (FLNC) | ENSP00000327145.8:p.Thr2697= | |
ENST00000346177.6:c.7992T>C (FLNC) | ENSP00000344002.6:p.Thr2664= | |
NM_001127487.1:c.7992T>C (FLNC) | NP_001120959.1:p.Thr2664= | |
NM_001458.4:c.8091T>C , LRG_870t1:c.8091T>C (FLNC) | NP_001449.3:p.Thr2697= | |
NR_149055.1:n.102+4089A>G (FLNC-AS1) | ||
NM_001127487.2:c.7992T>C (FLNC) | NP_001120959.1:p.Thr2664= | |
NM_001458.5:c.8091T>C (FLNC) MANE Select | NP_001449.3:p.Thr2697= |