HGVS | Genome Assembly |
---|---|
NC_000002.12:g.44942013_44942045del , CM000664.2:g.44942013_44942045del | GRCh38 |
NC_000002.11:g.45169152_45169184del , CM000664.1:g.45169152_45169184del | GRCh37 |
NC_000002.10:g.45022656_45022688del | NCBI36 |
NG_016222.1:g.5116_5148del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260653.5:c.-92_-60del MANE Select | ENSP00000260653.3:n.-92_-60del | |
ENST00000260653.4:c.-92_-60del | ENSP00000260653.3:n.-92_-60del | |
NM_005413.3:c.-92_-60del | NP_005404.1:n.-92_-60del | |
XM_011533042.1:c.-92_-60del | XP_011531344.1:n.-92_-60del | |
NM_005413.4:c.-92_-60del MANE Select | NP_005404.1:n.-92_-60del |