HGVS | Genome Assembly |
---|---|
NC_000016.10:g.86510594del , CM000678.2:g.86510594del | GRCh38 |
NC_000016.9:g.86544200del , CM000678.1:g.86544200del | GRCh37 |
NC_000016.8:g.85101701del | NCBI36 |
NG_016273.1:g.5068del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262426.6:c.25del MANE Select | ENSP00000262426.4:p.Gln9SerfsTer? | |
ENST00000262426.5:c.25del | ENSP00000262426.4:p.Gln9SerfsTer? | |
NM_001451.2:c.25del | NP_001442.2:p.Gln9SerfsTer? | |
NM_001451.3:c.25del MANE Select | NP_001442.2:p.Gln9SerfsTer? |