HGVS | Genome Assembly |
---|---|
NC_000001.11:g.45500302del , CM000663.2:g.45500302del | GRCh38 |
NC_000001.10:g.45965974del , CM000663.1:g.45965974del | GRCh37 |
NC_000001.9:g.45738561del | NCBI36 |
NG_013378.1:g.5119del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401061.9:c.-31del MANE Select | ENSP00000383840.4:n.-31del | |
ENST00000401061.8:c.-31del | ENSP00000383840.4:n.-31del | |
NM_015506.2:c.-31del | NP_056321.2:n.-31del | |
NM_001330540.1:c.-253del | NP_001317469.1:n.-253del | |
XM_005270724.5:c.-31del | XP_005270781.1:n.-31del | |
NM_015506.3:c.-31del MANE Select | NP_056321.2:n.-31del | |
NM_001330540.2:c.-253del | NP_001317469.1:n.-253del |