HGVS | Genome Assembly |
---|---|
NC_000012.12:g.76347734T>A , CM000674.2:g.76347734T>A | GRCh38 |
NC_000012.11:g.76741514T>A , CM000674.1:g.76741514T>A | GRCh37 |
NC_000012.10:g.75265645T>A | NCBI36 |
NG_016357.1:g.5709A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650064.2:c.251A>T MANE Select | ENSP00000497413.1:p.Lys84Ile | |
ENST00000393262.3:c.251A>T | ENSP00000376946.3:p.Lys84Ile | |
NM_024685.3:c.251A>T | NP_078961.3:p.Lys84Ile | |
NM_024685.4:c.251A>T MANE Select | NP_078961.3:p.Lys84Ile |