HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10658629_10658630delinsTG , CM000682.2:g.10658629_10658630delinsTG | GRCh38 |
NC_000020.10:g.10639277_10639278delinsTG , CM000682.1:g.10639277_10639278delinsTG | GRCh37 |
NC_000020.9:g.10587277_10587278delinsTG | NCBI36 |
NG_007496.1:g.20417_20418delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.532_533delinsCA MANE Select | ENSP00000254958.4:p.His178= | |
ENST00000254958.9:c.532_533delinsCA | ENSP00000254958.4:p.His178= | |
ENST00000423891.6:n.398_399delinsCA | ||
NM_000214.2:c.532_533delinsCA | NP_000205.1:p.His178= | |
NM_000214.3:c.532_533delinsCA MANE Select | NP_000205.1:p.His178= |