HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584423_41584424insATTGGCATTGT , CM000679.2:g.41584423_41584424insATTGGCATTGT | GRCh38 |
NC_000017.10:g.39740675_39740676insATTGGCATTGT , CM000679.1:g.39740675_39740676insATTGGCATTGT | GRCh37 |
NC_000017.9:g.36994201_36994202insATTGGCATTGT | NCBI36 |
NG_008624.1:g.7472_7473insACAATGCCAAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000167586.7:c.609-11_609-10insACAATGCCAAT MANE Select | ENSP00000167586.6:n.609-11_609-10insACAAT... | |
ENST00000167586.6:c.609-11_609-10insACAATGCCAAT | ENSP00000167586.6:n.609-11_609-10insACAAT... | |
ENST00000476662.1:n.48_49insACAATGCCAAT | ||
NM_000526.4:c.609-11_609-10insACAATGCCAAT | NP_000517.2:n.609-11_609-10insACAATGCCAAT... | |
NM_000526.5:c.609-11_609-10insACAATGCCAAT MANE Select | NP_000517.3:n.609-11_609-10insACAATGCCAAT... |