HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169529737T= , CM000663.2:g.169529737T= | GRCh38 |
NC_000001.10:g.169498975T= , CM000663.1:g.169498975T= | GRCh37 |
NC_000001.9:g.167765599T= | NCBI36 |
NG_011806.1:g.61795A= , LRG_553:g.61795A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367797.9:c.5290A= MANE Select | ENSP00000356771.3:p.Met1764= | |
ENST00000367796.3:c.5305A= | ENSP00000356770.3:p.Met1769= | |
ENST00000367797.7:c.5290A= | ENSP00000356771.3:p.Met1764= | |
NM_000130.4:c.5290A= , LRG_553t1:c.5290A= | NP_000121.2:p.Met1764= | |
XM_017000660.2:c.4879A= | XP_016856149.1:p.Met1627= | |
NM_000130.5:c.5290A= MANE Select | NP_000121.2:p.Met1764= |