HGVS | Genome Assembly |
---|---|
NC_000002.12:g.223053114_223053123del , CM000664.2:g.223053114_223053123del | GRCh38 |
NC_000002.11:g.223917832_223917841del , CM000664.1:g.223917832_223917841del | GRCh37 |
NC_000002.10:g.223626076_223626085del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000281830.4:c.284_293del MANE Select | ENSP00000281830.5:p.Ser95CysfsTer3 | |
ENST00000281830.3:c.437_446del | ENSP00000281830.4:p.Ser146CysfsTer3 | |
ENST00000488477.2:n.75+840_75+849del | ||
NM_080671.3:c.437_446del | NP_542402.3:p.Ser146CysfsTer3 | |
NM_080671.4:c.284_293del MANE Select | NP_542402.4:p.Ser95CysfsTer3 |