HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94043493_94043494insA , CM000663.2:g.94043493_94043494insA | GRCh38 |
NC_000001.10:g.94509049_94509050insA , CM000663.1:g.94509049_94509050insA | GRCh37 |
NC_000001.9:g.94281637_94281638insA | NCBI36 |
NG_009073.1:g.82656_82657insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.3051-19_3051-18insT MANE Select | ENSP00000359245.3:n.3051-19_3051-18insT | |
ENST00000370225.3:c.3051-19_3051-18insT | ENSP00000359245.3:n.3051-19_3051-18insT | |
ENST00000536513.5:c.-64-3405_-64-3404insT | ENSP00000439707.2:n.-64-3405_-64-3404insT | |
NM_000350.2:c.3051-19_3051-18insT | NP_000341.2:n.3051-19_3051-18insT | |
NM_000350.3:c.3051-19_3051-18insT MANE Select | NP_000341.2:n.3051-19_3051-18insT |