HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25010195_25010196insAAACAAAA , CM000685.2:g.25010195_25010196insAAACAAAA | GRCh38 |
NC_000023.10:g.25028312_25028313insAAACAAAA , CM000685.1:g.25028312_25028313insAAACAAAA | GRCh37 |
NC_000023.9:g.24938233_24938234insAAACAAAA | NCBI36 |
NG_008281.1:g.10754_10755insTTTGTTTT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379044.5:c.1119+65_1119+66insTTTGTTTT MANE Select | ENSP00000368332.4:n.1119+65_1119+66insTTT... | |
ENST00000379044.4:c.1119+65_1119+66insTTTGTTTT | ENSP00000368332.4:n.1119+65_1119+66insTTT... | |
NM_139058.2:c.1119+65_1119+66insTTTGTTTT | NP_620689.1:n.1119+65_1119+66insTTTGTTTT | |
NM_139058.3:c.1119+65_1119+66insTTTGTTTT MANE Select | NP_620689.1:n.1119+65_1119+66insTTTGTTTT |