HGVS | Genome Assembly |
---|---|
NC_000018.10:g.59269143_59269144insAG , CM000680.2:g.59269143_59269144insAG | GRCh38 |
NC_000018.9:g.56936375_56936376insAG , CM000680.1:g.56936375_56936376insAG | GRCh37 |
NC_000018.8:g.55087355_55087356insAG | NCBI36 |
NG_013031.1:g.9251_9252insTC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000334889.4:c.902_903insTC MANE Select | ENSP00000334813.3:p.Ser302ProfsTer30 | |
ENST00000256852.7:c.*333_*334insTC | ENSP00000256852.7:n.*333_*334insTC | |
ENST00000334889.3:c.902_903insTC | ENSP00000334813.3:p.Ser302ProfsTer30 | |
NM_013435.2:c.902_903insTC | NP_038463.2:p.Ser302ProfsTer30 | |
NM_013435.3:c.902_903insTC MANE Select | NP_038463.2:p.Ser302ProfsTer30 |