HGVS | Genome Assembly |
---|---|
NC_000001.11:g.192812265_192812268del , CM000663.2:g.192812265_192812268del | GRCh38 |
NC_000001.10:g.192781395_192781398del , CM000663.1:g.192781395_192781398del | GRCh37 |
NC_000001.9:g.191048018_191048021del | NCBI36 |
NG_012800.1:g.8227_8230del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000235382.7:c.*669_*672del MANE Select | ENSP00000235382.5:n.*669_*672del | |
ENST00000235382.6:c.*669_*672del | ENSP00000235382.5:n.*669_*672del | |
NM_002923.3:c.*669_*672del | NP_002914.1:n.*669_*672del | |
NM_002923.4:c.*669_*672del MANE Select | NP_002914.1:n.*669_*672del |