HGVS | Genome Assembly |
---|---|
NC_000021.9:g.41756929_41756931delinsTGC , CM000683.2:g.41756929_41756931delinsTGC | GRCh38 |
NC_000021.8:g.43177089_43177091delinsTGC , CM000683.1:g.43177089_43177091delinsTGC | GRCh37 |
NC_000021.7:g.42050158_42050160delinsTGC | NCBI36 |
NG_032113.1:g.15159_15161delinsGCA | |
NG_032113.2:g.15159_15161delinsGCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000332512.8:c.183-115_183-113delinsGCA MANE Select | ENSP00000332454.3:n.183-115_183-113delinsGCA | |
ENST00000332512.7:c.183-115_183-113delinsGCA | ENSP00000332454.3:n.183-115_183-113delinsGCA | |
ENST00000352483.3:c.183-115_183-113delinsGCA | ENSP00000330161.2:n.183-115_183-113delinsGCA | |
NM_020639.2:c.183-115_183-113delinsGCA | NP_065690.2:n.183-115_183-113delinsGCA | |
NM_020639.3:c.183-115_183-113delinsGCA MANE Select | NP_065690.2:n.183-115_183-113delinsGCA |