HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586855_41586857del , CM000679.2:g.41586855_41586857del | GRCh38 |
NC_000017.10:g.39743107_39743109del , CM000679.1:g.39743107_39743109del | GRCh37 |
NC_000017.9:g.36996633_36996635del | NCBI36 |
NG_008624.1:g.5039_5041del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.-23_-21del MANE Select | ENSP00000167586.6:n.-23_-21del | |
ENST00000167586.6:c.-23_-21del | ENSP00000167586.6:n.-23_-21del | |
NM_000526.4:c.-23_-21del | NP_000517.2:n.-23_-21del | |
NM_000526.5:c.-23_-21del MANE Select | NP_000517.3:n.-23_-21del |