HGVS | Genome Assembly |
---|---|
NC_000001.11:g.11845736T= , CM000663.2:g.11845736T= | GRCh38 |
NC_000001.10:g.11905793T= , CM000663.1:g.11905793T= | GRCh37 |
NC_000001.9:g.11828380T= | NCBI36 |
NG_012926.1:g.7048A= , LRG_751:g.7048A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000400892.3:c.*1931T= (CLCN6) | ENSP00000496938.1:n.*1931T= | |
ENST00000446542.5:n.751T= (NPPA-AS1) | ||
ENST00000376480.7:c.*273A= (NPPA) MANE Select | ENSP00000365663.3:n.*273A= | |
ENST00000610706.1:c.*267A= (NPPA) | ENSP00000483195.1:n.*267A= | |
NM_006172.3:c.*273A= , LRG_751t1:c.*273A= (NPPA) | NP_006163.1:n.*273A= | |
NR_037806.1:n.1449T= (NPPA-AS1) | ||
NM_006172.4:c.*273A= (NPPA) MANE Select | NP_006163.1:n.*273A= |