HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367850C>A , CM000677.2:g.73367850C>A | GRCh38 |
NC_000015.9:g.73660191C>A , CM000677.1:g.73660191C>A | GRCh37 |
NC_000015.8:g.71447244C>A | NCBI36 |
NG_009063.1:g.6415G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.421G>T MANE Select | ENSP00000261917.3:p.Glu141Ter | |
ENST00000261917.3:c.421G>T | ENSP00000261917.3:p.Glu141Ter | |
NM_005477.2:c.421G>T | NP_005468.1:p.Glu141Ter | |
NM_005477.3:c.421G>T MANE Select | NP_005468.1:p.Glu141Ter |