HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586861_41586864dup , CM000679.2:g.41586861_41586864dup | GRCh38 |
NC_000017.10:g.39743113_39743116dup , CM000679.1:g.39743113_39743116dup | GRCh37 |
NC_000017.9:g.36996639_36996642dup | NCBI36 |
NG_008624.1:g.5040_5043dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.-22_-19dup MANE Select | ENSP00000167586.6:n.-22_-19dup | |
ENST00000167586.6:c.-22_-19dup | ENSP00000167586.6:n.-22_-19dup | |
NM_000526.4:c.-22_-19dup | NP_000517.2:n.-22_-19dup | |
NM_000526.5:c.-22_-19dup MANE Select | NP_000517.3:n.-22_-19dup |