HGVS | Genome Assembly |
---|---|
NC_000001.11:g.11845731G>T , CM000663.2:g.11845731G>T | GRCh38 |
NC_000001.10:g.11905788G>T , CM000663.1:g.11905788G>T | GRCh37 |
NC_000001.9:g.11828375G>T | NCBI36 |
NG_012926.1:g.7053C>A , LRG_751:g.7053C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000400892.3:c.*1926G>T (CLCN6) | ENSP00000496938.1:n.*1926G>T | |
ENST00000446542.5:n.746G>T (NPPA-AS1) | ||
ENST00000376480.7:c.*278C>A (NPPA) MANE Select | ENSP00000365663.3:n.*278C>A | |
ENST00000610706.1:c.*272C>A (NPPA) | ENSP00000483195.1:n.*272C>A | |
NM_006172.3:c.*278C>A , LRG_751t1:c.*278C>A (NPPA) | NP_006163.1:n.*278C>A | |
NR_037806.1:n.1444G>T (NPPA-AS1) | ||
NM_006172.4:c.*278C>A (NPPA) MANE Select | NP_006163.1:n.*278C>A |