HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320315T= , CM000667.2:g.159320315T= | GRCh38 |
NC_000005.9:g.158747323T= , CM000667.1:g.158747323T= | GRCh37 |
NC_000005.8:g.158679901T= | NCBI36 |
NG_009618.1:g.15159A= , LRG_71:g.15159A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.58A= | ENSP00000512849.1:p.Arg20= | |
ENST00000696751.1:c.*183A= | ENSP00000512850.1:n.*183A= | |
ENST00000231228.3:c.688A= MANE Select | ENSP00000231228.2:p.Arg230= | |
ENST00000231228.2:c.688A= | ENSP00000231228.2:p.Arg230= | |
NM_002187.2:c.688A= , LRG_71t1:c.688A= | NP_002178.2:p.Arg230= | |
NM_002187.3:c.688A= MANE Select | NP_002178.2:p.Arg230= |