HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160882236_160882239del , CM000663.2:g.160882236_160882239del | GRCh38 |
NC_000001.10:g.160852026_160852029del , CM000663.1:g.160852026_160852029del | GRCh37 |
NC_000001.9:g.159118650_159118653del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000326245.4:c.158-32_158-29del MANE Select | ENSP00000323587.3:n.158-32_158-29del | |
ENST00000326245.3:c.158-32_158-29del | ENSP00000323587.3:n.158-32_158-29del | |
ENST00000464077.1:n.60_63del | ||
NM_017625.2:c.158-32_158-29del | NP_060095.2:n.158-32_158-29del | |
NM_017625.3:c.158-32_158-29del MANE Select | NP_060095.2:n.158-32_158-29del |