HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128851492A>T , CM000669.2:g.128851492A>T | GRCh38 |
NC_000007.13:g.128491546A>T , CM000669.1:g.128491546A>T | GRCh37 |
NC_000007.12:g.128278782A>T | NCBI36 |
NG_011807.1:g.26064A>T , LRG_870:g.26064A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.5706A>T (FLNC) MANE Select | ENSP00000327145.8:p.Ala1902= | |
ENST00000325888.12:c.5706A>T (FLNC) | ENSP00000327145.8:p.Ala1902= | |
ENST00000346177.6:c.5607A>T (FLNC) | ENSP00000344002.6:p.Ala1869= | |
NM_001127487.1:c.5607A>T (FLNC) | NP_001120959.1:p.Ala1869= | |
NM_001458.4:c.5706A>T , LRG_870t1:c.5706A>T (FLNC) | NP_001449.3:p.Ala1902= | |
NR_149055.1:n.224T>A (FLNC-AS1) | ||
NM_001127487.2:c.5607A>T (FLNC) | NP_001120959.1:p.Ala1869= | |
NM_001458.5:c.5706A>T (FLNC) MANE Select | NP_001449.3:p.Ala1902= |