HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670207T>C , CM000666.2:g.68670207T>C | GRCh38 |
NC_000004.11:g.69535925T>C , CM000666.1:g.69535925T>C | GRCh37 |
NC_000004.10:g.69218520T>C | NCBI36 |
NG_052676.1:g.5570A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.412A>G MANE Select | ENSP00000341045.5:p.Met138Val | |
ENST00000338206.5:c.412A>G | ENSP00000341045.5:p.Met138Val | |
ENST00000616841.4:c.412A>G | ENSP00000482004.1:p.Met138Val | |
NM_001076.3:c.412A>G | NP_001067.2:p.Met138Val | |
NM_001076.4:c.412A>G MANE Select | NP_001067.2:p.Met138Val |