HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021730_94021731delinsAC , CM000663.2:g.94021730_94021731delinsAC | GRCh38 |
NC_000001.10:g.94487286_94487287delinsAC , CM000663.1:g.94487286_94487287delinsAC | GRCh37 |
NC_000001.9:g.94259874_94259875delinsAC | NCBI36 |
NG_009073.1:g.104419_104420delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4774-17_4774-16delinsGT MANE Select | ENSP00000359245.3:n.4774-17_4774-16delinsGT | |
ENST00000370225.3:c.4774-17_4774-16delinsGT | ENSP00000359245.3:n.4774-17_4774-16delinsGT | |
ENST00000460514.1:n.268-17_268-16delinsGT | ||
ENST00000536513.5:c.1150-17_1150-16delinsGT | ENSP00000439707.2:n.1150-17_1150-16delinsGT | |
NM_000350.2:c.4774-17_4774-16delinsGT | NP_000341.2:n.4774-17_4774-16delinsGT | |
NM_000350.3:c.4774-17_4774-16delinsGT MANE Select | NP_000341.2:n.4774-17_4774-16delinsGT |