HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858563G>T , CM000669.2:g.128858563G>T | GRCh38 |
NC_000007.13:g.128498617G>T , CM000669.1:g.128498617G>T | GRCh37 |
NC_000007.12:g.128285853G>T | NCBI36 |
NG_011807.1:g.33135G>T , LRG_870:g.33135G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.*40G>T (FLNC) MANE Select | ENSP00000327145.8:n.*40G>T | |
ENST00000325888.12:c.*40G>T (FLNC) | ENSP00000327145.8:n.*40G>T | |
ENST00000346177.6:c.*40G>T (FLNC) | ENSP00000344002.6:n.*40G>T | |
NM_001127487.1:c.*40G>T (FLNC) | NP_001120959.1:n.*40G>T | |
NM_001458.4:c.*40G>T , LRG_870t1:c.*40G>T (FLNC) | NP_001449.3:n.*40G>T | |
NR_149055.1:n.102+3962C>A (FLNC-AS1) | ||
NM_001127487.2:c.*40G>T (FLNC) | NP_001120959.1:n.*40G>T | |
NM_001458.5:c.*40G>T (FLNC) MANE Select | NP_001449.3:n.*40G>T |