HGVS | Genome Assembly |
---|---|
NC_000001.11:g.204165323_204165324delinsTG , CM000663.2:g.204165323_204165324delinsTG | GRCh38 |
NC_000001.10:g.204134451_204134452delinsTG , CM000663.1:g.204134451_204134452delinsTG | GRCh37 |
NC_000001.9:g.202401074_202401075delinsTG | NCBI36 |
NG_012122.1:g.6014_6015delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000272190.9:c.98+872_98+873delinsCA MANE Select | ENSP00000272190.8:n.98+872_98+873delinsCA... | |
ENST00000638118.1:c.-16-3161_-16-3160delinsCA | ENSP00000490307.1:n.-16-3161_-16-3160deli... | |
ENST00000272190.8:c.98+872_98+873delinsCA | ENSP00000272190.8:n.98+872_98+873delinsCA... | |
NM_000537.3:c.98+872_98+873delinsCA | NP_000528.1:n.98+872_98+873delinsCA | |
NM_000537.4:c.98+872_98+873delinsCA MANE Select | NP_000528.1:n.98+872_98+873delinsCA |