HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21001670del , CM000664.2:g.21001670del | GRCh38 |
NC_000002.11:g.21224542del , CM000664.1:g.21224542del | GRCh37 |
NC_000002.10:g.21078047del | NCBI36 |
NG_011793.1:g.47409del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.*65del MANE Select | ENSP00000233242.1:n.*65del | |
ENST00000616098.4:c.13755del | ENSP00000477990.1:n.13755del | |
NM_000384.2:c.*65del | NP_000375.2:n.*65del | |
XM_011532809.1:c.5870-2392del | XP_011531111.1:n.5870-2392del | |
NM_000384.3:c.*65del MANE Select | NP_000375.3:n.*65del |