HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734228_4734229del , CM000679.2:g.4734228_4734229del | GRCh38 |
NC_000017.10:g.4637523_4637524del , CM000679.1:g.4637523_4637524del | GRCh37 |
NC_000017.9:g.4584272_4584273del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*276_*277del MANE Select | ENSP00000293778.7:n.*276_*277del | |
ENST00000293778.10:c.*276_*277del | ENSP00000293778.6:n.*276_*277del | |
ENST00000576153.5:n.832_833del | ||
NM_022059.3:c.*276_*277del | NP_071342.2:n.*276_*277del | |
NM_022059.4:c.*276_*277del | NP_071342.2:n.*276_*277del | |
NM_001386809.1:c.*276_*277del MANE Select | NP_001373738.1:n.*276_*277del |