HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858428A= , CM000669.2:g.128858428A= | GRCh38 |
NC_000007.13:g.128498482A= , CM000669.1:g.128498482A= | GRCh37 |
NC_000007.12:g.128285718A= | NCBI36 |
NG_011807.1:g.33000A= , LRG_870:g.33000A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.8083A= (FLNC) MANE Select | ENSP00000327145.8:p.Thr2695= | |
ENST00000325888.12:c.8083A= (FLNC) | ENSP00000327145.8:p.Thr2695= | |
ENST00000346177.6:c.7984A= (FLNC) | ENSP00000344002.6:p.Thr2662= | |
NM_001127487.1:c.7984A= (FLNC) | NP_001120959.1:p.Thr2662= | |
NM_001458.4:c.8083A= , LRG_870t1:c.8083A= (FLNC) | NP_001449.3:p.Thr2695= | |
NR_149055.1:n.102+4097T= (FLNC-AS1) | ||
NM_001127487.2:c.7984A= (FLNC) | NP_001120959.1:p.Thr2662= | |
NM_001458.5:c.8083A= (FLNC) MANE Select | NP_001449.3:p.Thr2695= |