HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148827114_148827116del , CM000667.2:g.148827114_148827116del | GRCh38 |
NC_000005.9:g.148206677_148206679del , CM000667.1:g.148206677_148206679del | GRCh37 |
NC_000005.8:g.148186870_148186872del | NCBI36 |
NG_016421.1:g.5522_5524del | |
NG_016421.2:g.5522_5524del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.283_285del MANE Select | ENSP00000305372.4:p.Leu95del | |
ENST00000305988.5:c.283_285del | ENSP00000305372.4:p.Leu95del | |
NM_000024.5:c.283_285del | NP_000015.1:p.Leu95del | |
NM_000024.6:c.283_285del MANE Select | NP_000015.2:p.Leu95del |