HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128854029C>G , CM000669.2:g.128854029C>G | GRCh38 |
NC_000007.13:g.128494083C>G , CM000669.1:g.128494083C>G | GRCh37 |
NC_000007.12:g.128281319C>G | NCBI36 |
NG_011807.1:g.28601C>G , LRG_870:g.28601C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.6540C>G (FLNC) MANE Select | ENSP00000327145.8:p.Arg2180= | |
ENST00000325888.12:c.6540C>G (FLNC) | ENSP00000327145.8:p.Arg2180= | |
ENST00000346177.6:c.6441C>G (FLNC) | ENSP00000344002.6:p.Arg2147= | |
NM_001127487.1:c.6441C>G (FLNC) | NP_001120959.1:p.Arg2147= | |
NM_001458.4:c.6540C>G , LRG_870t1:c.6540C>G (FLNC) | NP_001449.3:p.Arg2180= | |
NR_149055.1:n.103-632G>C (FLNC-AS1) | ||
NM_001127487.2:c.6441C>G (FLNC) | NP_001120959.1:p.Arg2147= | |
NM_001458.5:c.6540C>G (FLNC) MANE Select | NP_001449.3:p.Arg2180= |