HGVS | Genome Assembly |
---|---|
NC_000016.10:g.74713331A= , CM000678.2:g.74713331A= | GRCh38 |
NC_000016.9:g.74747229A= , CM000678.1:g.74747229A= | GRCh37 |
NC_000016.8:g.73304730A= | NCBI36 |
NG_017070.1:g.66501T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219368.8:c.*859T= MANE Select | ENSP00000219368.3:n.*859T= | |
ENST00000219368.7:c.*859T= | ENSP00000219368.3:n.*859T= | |
ENST00000562145.1:n.1699T= | ||
NM_024306.4:c.*859T= | NP_077282.3:n.*859T= | |
XM_011523319.1:c.*859T= | XP_011521621.1:n.*859T= | |
XM_011523319.2:c.*859T= | XP_011521621.1:n.*859T= | |
NM_024306.5:c.*859T= MANE Select | NP_077282.3:n.*859T= |