HGVS | Genome Assembly |
---|---|
NC_000001.11:g.58782442T= , CM000663.2:g.58782442T= | GRCh38 |
NC_000001.10:g.59248114T= , CM000663.1:g.59248114T= | GRCh37 |
NC_000001.9:g.59020702T= | NCBI36 |
NG_047027.1:g.6672A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000710273.1:c.695A= | ENSP00000518166.1:p.His232= | |
ENST00000371222.4:c.629A= MANE Select | ENSP00000360266.2:p.His210= | |
ENST00000678696.1:c.629A= | ENSP00000503132.1:p.His210= | |
ENST00000371222.3:c.629A= | ENSP00000360266.2:p.His210= | |
NM_002228.3:c.629A= | NP_002219.1:p.His210= | |
NM_002228.4:c.629A= MANE Select | NP_002219.1:p.His210= |