HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367697C= , CM000677.2:g.73367697C= | GRCh38 |
NC_000015.9:g.73660038C= , CM000677.1:g.73660038C= | GRCh37 |
NC_000015.8:g.71447091C= | NCBI36 |
NG_009063.1:g.6568G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.574G= MANE Select | ENSP00000261917.3:p.Gly192= | |
ENST00000261917.3:c.574G= | ENSP00000261917.3:p.Gly192= | |
NM_005477.2:c.574G= | NP_005468.1:p.Gly192= | |
NM_005477.3:c.574G= MANE Select | NP_005468.1:p.Gly192= |