HGVS | Genome Assembly |
---|---|
NC_000002.12:g.241801863C>A , CM000664.2:g.241801863C>A | GRCh38 |
NC_000002.11:g.242741278C>A , CM000664.1:g.242741278C>A | GRCh37 |
NC_000002.10:g.242389951C>A | NCBI36 |
NG_046977.1:g.30039C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000192314.7:c.202C>A MANE Select | ENSP00000192314.6:p.Leu68Ile | |
ENST00000192314.6:c.202C>A | ENSP00000192314.6:p.Leu68Ile | |
NM_022134.2:c.202C>A | NP_071417.2:p.Leu68Ile | |
NM_022134.3:c.202C>A MANE Select | NP_071417.2:p.Leu68Ile |