HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320410G>A , CM000667.2:g.159320410G>A | GRCh38 |
NC_000005.9:g.158747418G>A , CM000667.1:g.158747418G>A | GRCh37 |
NC_000005.8:g.158679996G>A | NCBI36 |
NG_009618.1:g.15064C>T , LRG_71:g.15064C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.-38C>T | ENSP00000512849.1:n.-38C>T | |
ENST00000696751.1:c.*88C>T | ENSP00000512850.1:n.*88C>T | |
ENST00000231228.3:c.593C>T MANE Select | ENSP00000231228.2:p.Ala198Val | |
ENST00000231228.2:c.593C>T | ENSP00000231228.2:p.Ala198Val | |
NM_002187.2:c.593C>T , LRG_71t1:c.593C>T | NP_002178.2:p.Ala198Val | |
NM_002187.3:c.593C>T MANE Select | NP_002178.2:p.Ala198Val |