HGVS | Genome Assembly |
---|---|
NC_000009.12:g.114325813_114325815delinsGGA , CM000671.2:g.114325813_114325815delinsGGA | GRCh38 |
NC_000009.11:g.117088093_117088095delinsGGA , CM000671.1:g.117088093_117088095delinsGGA | GRCh37 |
NC_000009.10:g.116127914_116127916delinsGGA | NCBI36 |
NG_012108.1:g.7791_7793delinsGGA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000259396.9:c.541-479_541-477delinsGGA MANE Select | ENSP00000259396.8:n.541-479_541-477delins... | |
ENST00000259396.8:c.541-479_541-477delinsGGA | ENSP00000259396.8:n.541-479_541-477delins... | |
NM_000607.2:c.541-479_541-477delinsGGA | NP_000598.2:n.541-479_541-477delinsGGA | |
NM_000607.3:c.541-479_541-477delinsGGA | NP_000598.2:n.541-479_541-477delinsGGA | |
NM_000607.4:c.541-479_541-477delinsGGA MANE Select | NP_000598.2:n.541-479_541-477delinsGGA |