HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94043491_94043493del , CM000663.2:g.94043491_94043493del | GRCh38 |
NC_000001.10:g.94509047_94509049del , CM000663.1:g.94509047_94509049del | GRCh37 |
NC_000001.9:g.94281635_94281637del | NCBI36 |
NG_009073.1:g.82659_82661del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.3051-16_3051-14del MANE Select | ENSP00000359245.3:n.3051-16_3051-14del | |
ENST00000370225.3:c.3051-16_3051-14del | ENSP00000359245.3:n.3051-16_3051-14del | |
ENST00000536513.5:c.-64-3402_-64-3400del | ENSP00000439707.2:n.-64-3402_-64-3400del | |
NM_000350.2:c.3051-16_3051-14del | NP_000341.2:n.3051-16_3051-14del | |
NM_000350.3:c.3051-16_3051-14del MANE Select | NP_000341.2:n.3051-16_3051-14del |