HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992917_16992918insT , CM000670.2:g.16992917_16992918insT | GRCh38 |
NC_000008.10:g.16850426_16850427insT , CM000670.1:g.16850426_16850427insT | GRCh37 |
NC_000008.9:g.16894797_16894798insT | NCBI36 |
NG_015978.1:g.14248_14249insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*154_*155insA MANE Select | ENSP00000180166.5:n.*154_*155insA | |
ENST00000180166.5:c.*154_*155insA | ENSP00000180166.5:n.*154_*155insA | |
NM_019851.2:c.*154_*155insA | NP_062825.1:n.*154_*155insA | |
NM_019851.3:c.*154_*155insA MANE Select | NP_062825.1:n.*154_*155insA |