HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74749914A>T , CM000677.2:g.74749914A>T | GRCh38 |
NC_000015.9:g.75042255A>T , CM000677.1:g.75042255A>T | GRCh37 |
NC_000015.8:g.72829308A>T | NCBI36 |
NG_008431.1:g.32373A>T | |
NG_008431.2:g.32373A>T | |
NG_061543.1:g.6070A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343932.5:c.176A>T MANE Select | ENSP00000342007.4:p.Lys59Met | |
ENST00000343932.4:c.176A>T | ENSP00000342007.4:p.Lys59Met | |
NM_000761.4:c.176A>T | NP_000752.2:p.Lys59Met | |
NM_000761.5:c.176A>T MANE Select | NP_000752.2:p.Lys59Met |